Research Associate II
Research associate job at Biomérieux
The Research Associate II position supports the performance assessment and validation of molecular in vitro diagnostic products within the Clinical Affairs Lab Operations team. This role contributes to regulatory submissions (e.g., FDA and global agencies) by executing molecular and microbiological experiments such as PCR, nucleic acid extraction, and microbial culture. The associate ensures data integrity through accurate collection, analysis, and documentation in compliance with protocols and safety standards. Operating in a collaborative, fast-paced environment, the role requires technical proficiency, critical thinking, and effective communication to support the department's mission and bioMérieux's goals. Responsible for creating, optimizing ,developing, updating and sustaining diagnostic assays and reagents in a regulated environment, while driving innovative solutions. Design and develop new biomolecules or reagents, collect and manage biological samples to support method/product development. Identify emerging technologies and trends related to diagnostics. Provide technical assistance to support existing products, methods or techniques. Performs analytical verifications and documenting validation activities and outcomes for regulatory submissions.
Primary Duties
1. Performs molecular and microbiological experiments (e.g., PCR, nucleic acid extraction, microbial culture) to support diagnostic product validation.
2. Ensures data integrity by collecting, recording, analyzing, and verifying experimental data in compliance with protocols and regulatory standards.
3. Executes study protocols and contributes to their development, optimization, and revision.
4. Conducts routine and complex calculations and laboratory techniques, including solution formulation and microbial enumeration.
5. Analyzes data with minimal supervision and determines appropriate next steps.
6. Communicates findings through written reports and oral presentations to peers and supervisors.
7. Contributes to the writing of study reports for internal and regulatory use.
8. Coordinates with team members and cross-functional groups for lab activities, equipment use, and project execution.
9. Maintains laboratory equipment, supplies, and workspaces according to safety and quality standards.
10. Trains other team members on lab practices and departmental procedures, as appropriate.
11. Develops troubleshooting strategies for unexpected experimental results and proposes solutions.
12. Operates in a Biosafety Level 2/2+ environment, handling pathogenic microbes and human specimens using sterile techniques.
13. Assists with inventory management and stocking of project-specific laboratory supplies.
14. Performs all work in compliance with corporate policies and the Quality Management System.15. Perform all work in compliance with company quality procedures and standards.16. Performs other duties as assigned.
Scope and Resources Accountability
The Research Associate II is an individual contributor with no direct or indirect supervisory responsibilities. The role operates within the Clinical Affairs Lab Operations team and is accountable for executing laboratory experiments, maintaining data integrity, and supporting regulatory submissions. The position requires coordination across functional groups and contributes to protocol development and troubleshooting, impacting the quality and timeliness of diagnostic product validation.
Key Performance Indicators (KPIs)
Accuracy and completeness of data recorded in lab notebooks and reports
Timely execution of study protocols and experiments
Compliance with safety, quality, and regulatory standards
Successful contribution to regulatory submissions (e.g., FDA)
Effective collaboration and communication within and across teams
Number of protocols executed or optimized
Training effectiveness for new team members
Qualifications
Education and Training
Bachelor's degree in a scientific discipline
Minimum of two years of post graduate experience in an academic, industry, or healthcare laboratory setting.Experience should include:
Real-time PCR
Sequence analysis
Microbiology techniques
Familiarity with Biosafety Level 2 practices
Knowledge, Skills, and Abilities
The role is primarily technical and scientific in nature, focused on laboratory work, data analysis, and regulatory support. There are no specific business strategy, financial, or market-facing responsibilities that require business acumen or understanding of broader business operations.
Develops strategies to troubleshoot unexpected experimental results and proposes innovative solutions.
Contributes to protocol and process development, optimization, and revision.
Demonstrates critical thinking and problem-solving skills to improve experimental design and product performance.
Evaluates primers and sequences using bioinformatic tools to support assay development.
Comfortable working in a dynamic environment where priorities may shift, requiring adaptability and creative thinking.These skills reflect the ability to innovate within scientific and technical domains, particularly in developing and refining diagnostic tools.
Maintaining Focus
Detail-oriented in executing laboratory procedures and maintaining accurate records.
Ability to follow rules and regulations, including protocols, SOPs, and safety guidelines.
Proficiency in laboratory practices, such as sterile technique, pipetting, and contamination control.
Comfortable working in a dynamic environment with shifting priorities, requiring sustained attention and adaptability.
Strong organizational skills to manage multiple tasks and maintain consistency in data collection and analysis.
Ability to remain in a stationary position (often standing) for prolonged periods, supporting physical focus during lab work. Getting Organized
Strong organizational skills to manage multiple tasks, experiments, and documentation efficiently.
Proficiency in inventory management, including stocking and tracking project-specific laboratory supplies.
Ability to maintain laboratory equipment, supplies, and workspaces in accordance with operational, safety, and quality standards.
Detail-oriented record keeping, including accurate data entry in electronic lab notebooks and study worksheets.
Ability to follow structured protocols and standard operating procedures to ensure consistency and compliance.
Comfortable working in a dynamic environment, requiring prioritization and time management. Getting Work Done Through Others
Trains other team members on laboratory and departmental practices and procedures, commensurate with experience.
Coordinates and collaborates within and across teams and functional groups for routine lab activities, equipment use, and project execution.
Shares knowledge, skills, and ideas to support team development and collective success.These responsibilities reflect the ability to support and guide others in completing work, even though the role does not include formal supervisory duties. Managing Work Processes Ability to follow structured protocols, SOPs, and work instruction documents to ensure consistency and compliance.
Maintains laboratory equipment, supplies, and workspaces according to operational, safety, and quality standards.
Ensures data integrity through accurate collection, analysis, and documentation of experimental results.
Executes study protocols and contributes to their development, optimization, and revision.
Performs routine and complex lab techniques with minimal supervision, demonstrating independence in managing assigned tasks.
Comfortable working in a dynamic environment, managing shifting priorities and timelines effectively. Dealing with Complex Situations
Demonstrated critical thinking and problem-solving skills to interpret experimental results and troubleshoot issues.
Develops strategies to address unexpected experimental outcomes and proposes scientifically sound solutions.
Comfortable working with biosafety level 2/2+ pathogens and human specimens, requiring careful risk assessment and adherence to safety protocols.
Ability to work independently on routine tasks and with general supervision on new or complex procedures.
Proficiency in data analysis and bioinformatics tools to evaluate sequences and interpret molecular biology results.
Adaptability in a dynamic environment, managing shifting priorities and complex workflows.
Communicates and coordinates effectively and respectfully with peers and supervisors across teams and functional groups.
Collaborates within and across departments, demonstrating awareness of team dynamics and shared goals.
Acts as a good lab citizen, contributing to a positive and productive work environment.
Understands and adheres to company policies, quality systems, and regulatory requirements, reflecting alignment with organizational standards and expectations.These abilities support effective navigation within the organizational structure and contribute to team cohesion and operational success.
Communicating Effectively
Strong oral and written communication skills for presenting data, writing reports, and collaborating with peers and supervisors.
Ability to communicate data and analyses clearly in written reports and oral presentations.
Collaborates respectfully and effectively within and across teams and functional groups.
Shares knowledge, skills, and ideas to support team learning and cohesion.
Comfortable using Microsoft Office tools (Outlook, Excel, PowerPoint, Word) to support communication and documentation.
Relating Skills
Collaborates effectively within and across teams and functional groups.
Communicates respectfully with peers and supervisors to support a positive and productive work environment.
Acts as a good lab citizen, demonstrating teamwork, accountability, and shared responsibility.
Shares knowledge, skills, and ideas to foster learning and cooperation among team members.
Trains other team members on laboratory and departmental practices, contributing to team development. Developing and Inspiring Others
Trains other team members on laboratory and departmental practices and procedures, commensurate with experience.
Shares knowledge, skills, and ideas to support team learning and development.
Acts as a collaborative team member, contributing to a positive and inclusive lab environment that encourages growth and knowledge exchange.While the role does not include formal leadership or supervisory responsibilities, it supports peer development through mentorship and skill-sharing. Managing Diverse Relationships
Collaborates effectively across teams and functional groups, demonstrating adaptability in working with individuals from various scientific and operational backgrounds.
Communicates respectfully and professionally with peers and supervisors to maintain productive working relationships.
Shares knowledge and skills to support team learning and cross-functional coordination.
Operates within a regulated environment, requiring interaction with internal stakeholders such as Quality Assurance, Regulatory Affairs, and R&D.
Acting with Honor and Being Open
Demonstrates integrity and accountability by ensuring data accuracy and compliance with protocols, SOPs, and regulatory standards.
Follows company policies and quality management guidelines, reflecting ethical conduct and transparency in work practices.
Communicates respectfully and professionally with peers and supervisors, fostering a culture of openness and trust.
Comfortable working with human specimens and biosafety level 2 pathogens, requiring adherence to safety and ethical standards.
Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bio Merieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site ******************************* or contact us at [email protected].
BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux's or its affiliates' application process by contacting us via telephone at **************, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).
Auto-ApplyScientist I
Research associate job at Biomérieux
This is a full time exempt position. Responsible for initiating, directing and executing scientific research and/or development strategies for BFDX through a research staff or individual studies. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, productions and problems. Familiar with a variety of the field's concepts, practices, and procedures including but not limited to PCR, RT-PCR real-time PCR, and use of fluorescence-based nucleic acid detection techniques. May receive general instructions on routine work, detailed instructions on new assignments.
Principal Job Duties and Responsibilities:
* Apply deep knowledge of fundamental physical principles to design, conduct, and interpret experiments with precision.
* Proficient in coded quantitative analysis using R, Python, and similar programming languages to extract insights from complex datasets.
* Skilled in understanding, structuring, and manipulating diverse data formats to streamline data collection, integration, and analysis.
* Perform all work in compliance with company policy and within the guidelines of BFDX's Quality System.
* Plans and executes laboratory research.
* Work involves development of new instrumentation, software or processes, customer support and some training functions.
* Maintains broad knowledge of state-of-the-art principles and theories.
* Makes contributions to literature and conferences.
* May advise top management on corporate research and development.
* Participates in development of patent applications.
* Responsible for development of research groups.
* Requires interaction with various company departments.
* Uses professional concepts to contribute to the development of company concepts and principles and to achieve objectives in creative and effective ways.
* Demonstrates potential for technical proficiency, scientific creativity, collaboration with others, and independent thought.
* Ensures that laboratory notebooks for assigned projects/experiments are maintained in accordance with BFDX Employment Handbook.
Qualifications:
Research Scientist PhD-RN
Saint Louis, MO jobs
Additional Information About the Role
A research scientist is a doctoral prepared clinician that educates, mentors and consults for healthcare professionals, as well as conducts projects across the trajectory of scholarly work (PI, QI, EBP and Research) to improve patient outcomes and experience. The research scientist provides guidance and assistance for dissemination of scholarly work.
PhD in Nursing required, or DNS.
Active MO RN License Required
Position is based onsite at Barnes Jewish Hospital
Supports Magnet facilty
Overview
Preferred Qualifications
Role Purpose
Develops the health services research program. Facilitates and independently conducts academic/clinical research, supports research utilization in nursing/clinical practice and develops an ongoing strategic plan for academic/clinical research.
Responsibilities
Conducts interdisciplinary research and evidence-based practice projects that support the organization's priorities for improving patient and/or care delivery outcomes.
Serves in a consultative role for patient care services staff in the development and completion of interdisciplinary research and evidence based practice projects and scholarly activities.
Collaborates with patient care services clinicians, including physician partners, to evaluate and implement best practices for clinical care, patient care delivery models, education and use of technology.
Mentors nursing and allied health professionals in developing presentations, posters and written articles or abstracts.
Presents original research and evidence based practice at regional and national conferences with poster or podium presentations and submits for publication in peer-review journals.
Minimum Requirements
Education
Doctorate
- Nursing/Healthcare related
Experience
5-10 years
Supervisor Experience
No Experience
Licenses & Certifications
Cert/Lic in Area of Expertise
Benefits and Legal Statement
BJC Total Rewards
At BJC we're committed to providing you and your family with benefits and resources to help you manage your physical, emotional, social and financial well-being.
Comprehensive medical, dental, vison, life insurance, and legal services available first day of the month after hire date
Disability insurance* paid for by BJC
Annual 4% BJC Automatic Retirement Contribution
401(k) plan with BJC match
Tuition Assistance available on first day
BJC Institute for Learning and Development
Health Care and Dependent Care Flexible Spending Accounts
Paid Time Off benefit combines vacation, sick days, holidays and personal time
Adoption assistance
To learn more, go to our Benefits Summary
*Not all benefits apply to all jobs
The above information on this description has been designed to indicate the general nature and level of work performed by employees in this position. It is not designed to contain or be interpreted as an exhaustive list of all responsibilities, duties and qualifications required of employees assigned to this job. Equal Opportunity Employer
Academic/Faculty/Research Physician
Charlotte, NC jobs
JOB DESCRIPTION:Medical center in North Carolina is seeking a BC/BE FM/OB physician to join a full scope Family Medicine academic residency practice. This will be a residency teaching position with a faculty appointment and includes outpatient precepting and rotation on inpatient service for up to 5 weeks per year.
Position Highlights:8 Physicians, 3 APPs, 6 FM Residents, support staff, and co-located behavioral health psychologist In house hospital call is approx.
1 night every 3 weeks supervising residents Office hours are Monday-Friday 8:00AM-5:00PMFull scope FM Clinic including maternity care Access to additional System level care management resources and virtual technology HOSPITAL:We are a regional 450-bed, not-for-profit hospital.
More than 4,200 hospital employees provide services through an extensive inpatient and outpatient network, including the Children's Hospital, Family Center, and Cancer Center.
You can work alongside the most advanced minds in medicine to improve medicine, elevate hope, and advance healing.
Practice where your voice is valued, your passion for advancing medicine is rewarded, and you get the resources and support you need to thrive.
COMMUNITY:Greater Charlotte, a vibrant city, which offers a plethora of cultural, social, and recreational activities, including museums, galleries, many restaurants, cafes, and more! The nearby community offers a very affordable cost of living, strong schools in both the public and private sector, and sits conveniently within equal distance between the Blue Ridge Mountains of NC and the beautiful Atlantic coast.
Outdoor enthusiasts will appreciate the area's wide array and abundance of wildlife, pristine forests, and hiking trails.
COME JOIN US! Apply now:For consideration or more information, please EMAIL CV to mailto: Telephone is tel: .
PLEASE REFERENCE JOB ID: -DCAF
Academic/Faculty/Research Physician
Kingston, PA jobs
Job Summary Geisinger Community Medicine is seeking a family medicine trained physician to join our team at Geisinger Kingston in Kingston, Pennsylvania. Become part of a nationally recognized health system that's redefining primary care-right in the heart of Northeast PA.
Job Duties
Make a Difference Where It Matters Most - Join Geisinger Pittston in Pittston, PA
What You'll Love About This Role:
Outpatient-only schedule with flexibility to fit your lifestyle
Collaborative care model with APP panel sharing
Robust support system:
Up-To-Date access
Behavioral health collaboration
24/7 nurse call center
Centralized prescription refill team
Value-based care guides
Epic EMR
' New ' Ambient voice dictation tool to streamline documentation and reduce clerical burden
We take pride in the support we provide our physicians:
$10k geography stipend guaranteed for two years
Compensation - competitive salary ranges from $320k to $375k based on experience
Up to $250k recruitment incentives
Residency/Fellowship stipend - up to 45k; available up to 18 months prior to graduation
Continuing medical education - 15 working days and $4,500 CME funds
Fully paid relocation
401k - Geisinger annually contributes over $15k
Academic involvement with medical students and residents
Learn more at,
Location Highlight - Kingston, PA
Nestled along the scenic Susquehanna River, Kingston offers the perfect blend of small-town charm and modern convenience. Located just minutes from Wilkes-Barre, this vibrant community boasts excellent schools, beautiful parks, and a welcoming atmosphere. With easy access to outdoor recreation, cultural attractions, and a variety of dining and shopping options, Kingston is an ideal place to live, work, and play.
Contact us:
Position Details
Education Doctor of Medicine or Doctor of Osteopathic Medicine- (Required)
Experience
Certification(s) and License(s) Licensed Medical Doctor - State of Pennsylvania
About Geisinger
Founded more than 100 years ago by Abigail Geisinger, the system now includes ten hospital campuses, a 550,000-member health plan, two research centers and the Geisinger Commonwealth School of Medicine. With nearly 24,000 employees and more than 1,700 employed physicians, Geisinger boosts its hometown economies in Pennsylvania by billions of dollars annually. Learn more at geisinger.org or connect with us on Facebook , Instagram , LinkedIn and Twitter .
Our Vision & Values
Everything we do is about making better health easier for our patients, our members, our students, our Geisinger family and our communities.
KINDNESS: We strive to treat everyone as we would hope to be treated ourselves.
EXCELLENCE: We treasure colleagues who humbly strive for excellence.
LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow.
INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation.
SAFETY: We provide a safe environment for our patients and members and the Geisinger family.
Our Benefits
We offer healthcare benefits for full time and part time positions from day one, including vision, dental and prescription coverage.
Academic/Faculty/Research Physician
Mifflintown, PA jobs
Job Summary Make a Difference Where It Matters MostJoin Geisinger Community Medicine in Mifflintown, PA, and become part of a nationally recognized health system that's redefining primary care. We're looking for Family Medicine physicians who are passionate about patient-centered care and ready to thrive in a supportive, innovative environment.
Job Duties
What You'll Love About This Role:
Outpatient-only schedule with flexibility to fit your lifestyle
Clinic hours:
Monday 7:00 AM - 6:00 PM
Tuesday 8:00 AM - 6:00 PM
Wednesday 7:00 AM - 5:00 PM
Thursday 7:00 AM - 5:00 PM
Friday 7:30 AM - 5:00 PM
One evening per week required
Saturday rotation required (approx. 1 in 6)
Schedule: 36 clinical and 4 administrative hours per week
Collaborative care model with APP panel sharing
Robust support system:
Up-To-Date access
Behavioral health collaboration
24/7 nurse call center
Centralized prescription refill team
Value-based care guides
Epic EMR
' New ' Ambient voice dictation tool to streamline documentation and reduce clerical burden
We take pride in the support we provide our physicians:
Compensation - competitive salary ranges from $320k to $375k based on experience
Up to $250k recruitment incentives
Residency/Fellowship stipend - up to 45k; available up to 18 months prior to graduation
Continuing medical education - 15 working days and $4,500 CME funds
Fully paid relocation
401k - Geisinger annually contributes over $15k
Academic involvement with medical students and residents
Learn more at,
Location Highlight - Mifflintown, PA
Scenic Beauty & Outdoor Recreation
Thousand Steps Trail: A challenging but rewarding hike offering breathtaking views of the Juniata River Valley.
Buttonwood Campground & Juniata River Adventures: Perfect for family-friendly camping, kayaking, and tubing along the Juniata River.
Cedar Springs Community Park: A peaceful spot for picnics, walks, and community events.
Small-Town Charm with Community Spirit
Mifflintown offers a tight-knit, welcoming community ideal for raising a family.
The area is known for its low cost of living, safe neighborhoods, and excellent public schools.
Local Culture & Attractions
Hazard's Distillery: A local gem offering handcrafted spirits and a cozy tasting room.
Historic Juniata County Courthouse: A beautiful landmark in the heart of town.
Nearby Lewistown: Just a short drive away, it features cultural sites like the Embassy Theatre, Monument Square, and the McCoy House Museum.
Convenient Location
Centrally located in Pennsylvania, Mifflintown is within easy driving distance to Harrisburg, State College, and Altoona, offering access to urban amenities while enjoying rural tranquility.
Cultural Richness
The region is home to a vibrant Amish and Mennonite community, adding to its cultural depth and offering unique local markets and handmade goods.
Position Details
Education Doctor of Medicine or Doctor of Osteopathic Medicine- (Required)
Experience
Certification(s) and License(s) Licensed Medical Doctor - State of Pennsylvania
About Geisinger
Founded more than 100 years ago by Abigail Geisinger, the system now includes ten hospital campuses, a 550,000-member health plan, two research centers and the Geisinger Commonwealth School of Medicine. With nearly 24,000 employees and more than 1,700 employed physicians, Geisinger boosts its hometown economies in Pennsylvania by billions of dollars annually. Learn more at geisinger.org or connect with us on Facebook , Instagram , LinkedIn and Twitter .
Our Vision & Values
Everything we do is about making better health easier for our patients, our members, our students, our Geisinger family and our communities.
KINDNESS: We strive to treat everyone as we would hope to be treated ourselves.
EXCELLENCE: We treasure colleagues who humbly strive for excellence.
LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow.
INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation.
SAFETY: We provide a safe environment for our patients and members and the Geisinger family.
Our Benefits
We offer healthcare benefits for full time and part time positions from day one, including vision, dental and prescription coverage.
Research Associate
Chicago, IL jobs
Research Associate - R&D Compensation: $60K - $85K salary + 0.1% - 0.2% equity + benefits BiomeSense is a start-up revolutionizing human gut microbiome sampling and analysis, driving discovery, and enabling the development of microbiome-based precision medicine. Our innovative approach integrates two core advancements: hardware that facilitates daily microbiome sampling as a routine exercise, and AI-driven analytics to unlock novel datasets for biomarker discovery.
We are seeking a Research Associate to join our Research and Development team. This is a unique opportunity to apply your technical skills and collaborative spirit in a dynamic, fast-paced environment. As part of our scientific team, you will help advance our automated sample processing workflows, supporting the foundation of our sample-to-answer multi-omic platform technology.
Key Responsibilities
Laboratory Execution & Technical Support:
Execute and optimize microbiology protocols supporting nucleic acid extraction, PCR, next-generation sequencing (NGS), in a high-throughput laboratory environment.
Collaborate closely with engineers, scientists, and product teams to validate and integrate novel systems for microbial DNA stabilization, extraction, and purification.
Coordinate and execute the processing of large quantities of partner samples, maintaining a strong focus on accuracy and efficiency.
Design and conduct experiments to retire technical risks or optimize laboratory protocols, contributing to ongoing process improvements and product innovation.
Quality & Communication:
Maintain rigorous documentation practices and adhere to established quality management systems (e.g., GLP, design controls).
Effectively communicate experimental results and technical observations to cross-functional project teams, supporting the rapid advancement of platform technologies.
Qualifications
Bachelor's degree + 3 years', or Master's degree + 2 years' in biological sciences, bioengineering, or a related field.
Hands-on experience with core microbiology techniques, nucleic acid extraction, PCR, and NGS sample preparation.
Highly organized, proactive, and able to thrive in a collaborative, fast-paced setting.
Strong communication skills for clear reporting and knowledge-sharing with scientific and technical stakeholders.
Auto-ApplyResearch Associate II, Bioanalytical
Durham, NC jobs
AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
* Advance innovative science by pushing boundaries.
* Bring transformative therapeutics to patients in need.
* Provide an environment for employees to reach their fullest potential.
Our values:
* Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
* Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
* Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
* Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
* Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.
The Research Associate II, Bioanalytical, will report to the Director, Translational Biomarkers, and will participate in the development, qualification, validation, and execution of assays investigating biodistribution, viral shedding, and functional assessments in support of pre-clinical and clinical stage programs. This is an on-site lab-based position in Morrisville, NC and prior experience with methods for extraction and quantification of nucleic material (DNA, RNA) and protein is required. The ideal candidate would have knowledge of various molecular techniques to quantify transgene expression. Candidates may also have opportunities to learn different techniques for protein assessment. Experience with GxP regulation and working in a regulated lab space is preferred but not required.
Job Responsibilities
* Isolate and quantify nucleic acids and proteins from various model systems and tissue types
* Participate in assay design, including assay qualification and validation
* Utilize molecular techniques including, but not limited to gene expression analysis, primer probe set design/validation, dd PCR, RT-dd PCR, ELISA, western blots, and MSD for sample analysis
* Responsible for co-authoring and reviewing test methods, work plans, SOPs, and qualification/validation reports
* Contribute to data review and quality control of data in support of regulatory filings
* Perform routine instrument maintenance and performance verification
* Maintain organized electronic and/or paper-based documentation that is fit-for-purpose with regards to regulatory requirements.
* Receive, accession, and manage samples using LIMS
* Perform data analysis and effectively communicate results in formal reports and presentations for technical discussions
* Maintain inventories and/or place orders of reagents and materials needed for the assigned projects allowing for timely execution of related lab work
* Ensure lab areas are clean and organized, and that equipment, supplies, and raw materials are available for use
Minimum Requirements
* Master's degree in biology, chemistry or related field OR bachelor's degree in biology, chemistry, or related field with 2+ years' relevant work experience OR High School Diploma and 6+ years' relevant work experience
* Hands-on experience with the processing of, and isolation of nucleic acids and protein from, material acquired from different species and organ types
* Demonstrated understanding of assay qualification and/or validation requirements
* Possess knowledge of, and experience with, multiple assays including: dd PCR, RT-dd PCR, ELISA, western blots, and/or MSD-based platforms
* Excellent technical lab skills with attention to detail and the ability to assume independent ownership of workflows
* Knowledge of GxP regulatory requirements
* Ability to multitask among multiple projects and teams, and work in a fast-paced, highly interactive environment
* Self-motivated, organized, and capable of troubleshooting independently
* Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
* Excellent communication skills with ability to collaborate with colleagues across multiple communication platforms including e-mail, Microsoft Teams, and Sharepoint sites
Preferred Education, Experience, and Skills
* Hands-on experience with assay qualification and validation
* Prior work in a regulated lab environment
* Familiarity with software such as Softmax Pro, graphpad prism, and smartsheet
* Prior use of LIMS sample management software and/or lab automation
* Relevant knowledge and industrial experience with gene therapy, including AAV and/or lentiviral-based platforms
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job‐related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at ************** or sending us an email at ******************.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.
Research Associate II, Bioanalytical
Durham, NC jobs
AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
* Advance innovative science by pushing boundaries.
* Bring transformative therapeutics to patients in need.
* Provide an environment for employees to reach their fullest potential.
Our values:
* Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
* Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
* Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
* Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
* Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.
Position Summary
The Research Associate II, Bioanalytical, will report to the Director, Translational Biomarkers, and will participate in the development, qualification, validation, and execution of assays investigating biodistribution, viral shedding, and functional assessments in support of pre-clinical and clinical stage programs. This is an on-site lab-based position in Morrisville, NC and prior experience with methods for extraction and quantification of nucleic material (DNA, RNA) and protein is required. The ideal candidate would have knowledge of various molecular techniques to quantify transgene expression. Candidates may also have opportunities to learn different techniques for protein assessment. Experience with GxP regulation and working in a regulated lab space is preferred but not required.
Job Responsibilities
* Isolate and quantify nucleic acids and proteins from various model systems and tissue types
* Participate in assay design, including assay qualification and validation
* Utilize molecular techniques including, but not limited to gene expression analysis, primer probe set design/validation, dd PCR, RT-dd PCR, ELISA, western blots, and MSD for sample analysis
* Responsible for co-authoring and reviewing test methods, work plans, SOPs, and qualification/validation reports
* Contribute to data review and quality control of data in support of regulatory filings
* Perform routine instrument maintenance and performance verification
* Maintain organized electronic and/or paper-based documentation that is fit-for-purpose with regards to regulatory requirements.
* Receive, accession, and manage samples using LIMS
* Perform data analysis and effectively communicate results in formal reports and presentations for technical discussions
* Maintain inventories and/or place orders of reagents and materials needed for the assigned projects allowing for timely execution of related lab work
* Ensure lab areas are clean and organized, and that equipment, supplies, and raw materials are available for use
Minimum Requirements
* Master's degree in biology, chemistry or related field OR bachelor's degree in biology, chemistry, or related field with 2+ years' relevant work experience OR High School Diploma and 6+ years' relevant work experience
* Hands-on experience with the processing of, and isolation of nucleic acids and protein from, material acquired from different species and organ types
* Demonstrated understanding of assay qualification and/or validation requirements
* Possess knowledge of, and experience with, multiple assays including: dd PCR, RT-dd PCR, ELISA, western blots, and/or MSD-based platforms
* Excellent technical lab skills with attention to detail and the ability to assume independent ownership of workflows
* Knowledge of GxP regulatory requirements
* Ability to multitask among multiple projects and teams, and work in a fast-paced, highly interactive environment
* Self-motivated, organized, and capable of troubleshooting independently
* Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
* Excellent communication skills with ability to collaborate with colleagues across multiple communication platforms including e-mail, Microsoft Teams, and Sharepoint sites
Preferred Education, Experience, and Skills
* Hands-on experience with assay qualification and validation
* Prior work in a regulated lab environment
* Familiarity with software such as Softmax Pro, graphpad prism, and smartsheet
* Prior use of LIMS sample management software and/or lab automation
* Relevant knowledge and industrial experience with gene therapy, including AAV and/or lentiviral-based platforms
AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job‐related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at ************** or sending us an email at ******************.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.
Cultivation Research Genetics Associate
Chambersburg, PA jobs
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our
Rooted in Good
initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Title: Cultivation Associate
Pay Range: $17
Location: Chambersburg, PA
Job Type: Full Time | Non-Exempt
Shift: Monday - Friday, 7:15 am - 3:45 pm
Who You Are: You're passionate about cannabis science and curious about how plants work at the cellular level. You have hands-on experience with cultivation, tissue culture, or micropropagation and are eager to expand your skills in genetic research and plant development. You're precise, organized, and comfortable working in a controlled lab-based environment where attention to detail and data accuracy are key. What You'll Do: As a Cultivation Research Genetics Associate at Curaleaf's Research & Development facility, you'll contribute to our cutting-edge genetics program - working to advance plant performance, consistency, and innovation. This role blends lab and cultivation responsibilities, supporting projects focused on cellular genetics, tissue culture, and strain development. Your day will include:
Supporting genetic and cellular research, including micropropagation, tissue culture, and cellular sample preservation
Performing audits on cellular samples to ensure quality, accuracy, and data integrity
Maintaining detailed records of genetic trials, cell lines, and environmental conditions
Assisting with propagation, growth trials, and phenotype tracking as part of the genetics program
Operating and maintaining laboratory equipment, including microscopes, cryogenic storage systems, and sterilization tools
Following aseptic techniques and maintaining clean lab environments to prevent contamination
Collaborating with cultivation and R&D teams to connect lab-based findings with live plant trials
Accurately labeling and tracking plant materials and samples in accordance with state compliance regulations
Pitching in during high-demand periods to support broader cultivation or processing projects as needed
What You'll Bring:
A strong passion for cannabis genetics, biology, or plant science
Prior experience with plant micropropagation, cellular analysis, or laboratory procedures
Understanding of sterile technique, sample handling, and controlled-environment workflows
Flexibility to work across both North and Central Phoenix facilities as needed
Sharp attention to detail with a focus on precision, cleanliness, and documentation
Reliability, organization, and time management skills to balance multiple ongoing projects
A high school diploma or GED required; coursework in biology, horticulture, plant science, or biotechnology preferred
Even Better If:
You have direct experience with cannabis tissue culture or genetic preservation
You've worked in a plant science or biotech lab supporting genetic research or quality control
You bring knowledge of plant physiology, breeding, and advanced cultivation techniques
Physical Requirements:
Ability to stand, sit, and walk for extended periods (8-10 hours per shift)
Ability to lift and carry up to 50 pounds with or without assistance
Frequent bending, squatting, and reaching
Fine motor skills and steady hand-eye coordination for lab work
Use of PPE including lab coats, gloves, masks, hair nets, and non-slip shoes
Environmental Conditions:
Lab and cultivation environments with controlled temperature and humidity
Exposure to cleaning solvents, isopropyl alcohol, and lab sterilization materials
Possible exposure to strong odors (such as cannabis)
Bright lighting and equipment noise typical of lab or production settings
Curaleaf Pay Transparency
$17 - $17 USD
What We Offer:
Career Growth Opportunities
Competitive Pay and Benefits
Generous PTO and Parental Leave
401(K) Retirement Plan
Life/ Disability Insurance
Community Involvement
Referral Bonuses and Product Discounts
Benefits vary by state, role type, and eligibility.
Follow us on Social Media:
Instagram: @curaleaf.usa
Twitter: @Curaleaf_Inc
LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis.
Our Values:
Lead and Inspire.
Commit to Win.
ONE Curaleaf.
Driven to Deliver Excellence.
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.
Auto-ApplyCultivation Research Genetics Associate
Chambersburg, PA jobs
Job Description
At Curaleaf, we're redefining the cannabis industry with a strong commitment to quality, expertise, and innovation. As a leading global cannabis provider, our brands-including Curaleaf, Select, and Grassroots-offer premium products and services in both medical and adult-use markets.
Join us at Curaleaf to be part of a high-growth, purpose-driven company that champions corporate social responsibility through our
Rooted in Good
initiative, supporting community outreach and positive change. Here, you'll have the opportunity to make a meaningful impact, drive innovation, and help shape the future of cannabis.
Title: Cultivation Associate
Pay Range: $17
Location: Chambersburg, PA
Job Type: Full Time | Non-Exempt
Shift: Monday - Friday, 7:15 am - 3:45 pm
Who You Are:You're passionate about cannabis science and curious about how plants work at the cellular level. You have hands-on experience with cultivation, tissue culture, or micropropagation and are eager to expand your skills in genetic research and plant development. You're precise, organized, and comfortable working in a controlled lab-based environment where attention to detail and data accuracy are key.What You'll Do:As a Cultivation Research Genetics Associate at Curaleaf's Research & Development facility, you'll contribute to our cutting-edge genetics program - working to advance plant performance, consistency, and innovation. This role blends lab and cultivation responsibilities, supporting projects focused on cellular genetics, tissue culture, and strain development.Your day will include:
Supporting genetic and cellular research, including micropropagation, tissue culture, and cellular sample preservation
Performing audits on cellular samples to ensure quality, accuracy, and data integrity
Maintaining detailed records of genetic trials, cell lines, and environmental conditions
Assisting with propagation, growth trials, and phenotype tracking as part of the genetics program
Operating and maintaining laboratory equipment, including microscopes, cryogenic storage systems, and sterilization tools
Following aseptic techniques and maintaining clean lab environments to prevent contamination
Collaborating with cultivation and R&D teams to connect lab-based findings with live plant trials
Accurately labeling and tracking plant materials and samples in accordance with state compliance regulations
Pitching in during high-demand periods to support broader cultivation or processing projects as needed
What You'll Bring:
A strong passion for cannabis genetics, biology, or plant science
Prior experience with plant micropropagation, cellular analysis, or laboratory procedures
Understanding of sterile technique, sample handling, and controlled-environment workflows
Flexibility to work across both North and Central Phoenix facilities as needed
Sharp attention to detail with a focus on precision, cleanliness, and documentation
Reliability, organization, and time management skills to balance multiple ongoing projects
A high school diploma or GED required; coursework in biology, horticulture, plant science, or biotechnology preferred
Even Better If:
You have direct experience with cannabis tissue culture or genetic preservation
You've worked in a plant science or biotech lab supporting genetic research or quality control
You bring knowledge of plant physiology, breeding, and advanced cultivation techniques
Physical Requirements:
Ability to stand, sit, and walk for extended periods (8-10 hours per shift)
Ability to lift and carry up to 50 pounds with or without assistance
Frequent bending, squatting, and reaching
Fine motor skills and steady hand-eye coordination for lab work
Use of PPE including lab coats, gloves, masks, hair nets, and non-slip shoes
Environmental Conditions:
Lab and cultivation environments with controlled temperature and humidity
Exposure to cleaning solvents, isopropyl alcohol, and lab sterilization materials
Possible exposure to strong odors (such as cannabis)
Bright lighting and equipment noise typical of lab or production settings
Curaleaf Pay Transparency$17-$17 USD
What We Offer:
Career Growth Opportunities
Competitive Pay and Benefits
Generous PTO and Parental Leave
401(K) Retirement Plan
Life/ Disability Insurance
Community Involvement
Referral Bonuses and Product Discounts
Benefits vary by state, role type, and eligibility.
Follow us on Social Media:
Instagram: @curaleaf.usa
Twitter: @Curaleaf_Inc
LinkedIn: Curaleaf LinkedIn
Curaleaf Holdings, Inc. (TSX: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis with a mission to enhance lives by cultivating, sharing, and celebrating the power of the plant. As a high-growth cannabis company known for quality, expertise and reliability, the Company, and its brands, including Curaleaf, Select, Grassroots, JAMS, Find and Zero Proof provide industry-leading service, product selection and accessibility across the medical and adult-use markets. Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our Vision: To be the world's leading cannabis company by consistently delivering superior products and services and driving the global acceptance of cannabis.
Our Values:
Lead and Inspire.
Commit to Win.
ONE Curaleaf.
Driven to Deliver Excellence.
Curaleaf is an equal opportunity employer. Curaleaf recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, gender identity, sexual orientation, physical ability, age, veteran status, and other protected status as required by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Individuals adversely impacted by the war on drugs are encouraged to apply.
Current Curaleaf employees should apply for open positions through our Internal Job Board, which can be accessed via the link on The Leaf.
Research Associate I
Durham, NC jobs
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position Summary:
Join a highly technical analytical team in a dynamic work environment where you will participate in contracted client analytical programs as a member of the Analytical Development (AD) Department. The individual in this position will be responsible for executing experimental protocols and performing data analysis in biopharmaceutical laboratories.
Position Responsibilities:
Performs testing on in-process, drug substance/drug product, or formulation samples using bio-analytical techniques such as (but not limited to) HPLC, SDS-PAGE, SDS-CGE, ELISA, UV-Vis, and/or biophysical characterization techniques. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals
Makes detailed observations and carries out elementary data analysis.
Understands experiments and conducts troubleshooting analysis.
Maintains and updates knowledge of instrumentation.
Electronic notebook upkeep and writing skills.
Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature.
Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste.
Reacts to change productively and handles other essential tasks as assigned.
Minimum Requirements:
Research Associate I requires a Bachelor's degree in chemistry, biochemistry or related area (or equivalent training) with 0+ years of relevant experience
Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables.
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.
Salary Range:
Research Associate I: $55,000-$70,000
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.
About KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit *********************
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
Auto-ApplyResearch Associate
Philadelphia, PA jobs
through the following https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=32012&clientkey=703E6F23E139A9E15CD4746A9D25637D&jpt=1b79bf1ead1b4f21088d5e********** The mission of the Health Federation of Philadelphia is to improve access to and quality of health care services for under served and vulnerable individuals and families.
Since 1983, The Health Federation has served as a network of the community health centers in Southeastern Pennsylvania, providing a forum for the region's federally qualified health centers and the Philadelphia Department of Public Health to collaborate and mobilize resources for their shared goals of improving the health of the population by expanding access to high quality care.
Job Description
JOB SUMMARY
Who we are:
The mission of the Philadelphia Department of Public Health (PDPH) is to protect and promote the health of all Philadelphians and to provide a safety net for the most vulnerable. Within PDPH, the Division of Chronic Disease and Injury Prevention (aka “Get Healthy Philly”), works to change policies, systems, and environments to make healthy living an easy choice for residents. The goals of our programs are to reduce obesity, smoking, and other known risk factors for chronic diseases. We are also expanding our injury prevention work, with a focus on reducing gun violence. The Division is especially concerned about documenting, understanding, and working to reduce disparities in health.
The Public Health Data Lab at Get Healthy Philly conducts innovative research and analysis that directly informs city policy and guides public health decisions. We provide the evidence base to answer questions like: Why do some neighborhoods have higher rates of cancer mortality than others? Will restrictions on the sale of certain tobacco products reduce the rate of teen vaping in Philadelphia? What policies or programs have worked to reduce gun violence in other communities, and could they work in Philadelphia?
Our values
: Get Healthy Philly's work is guided by our commitment to all people's health and humanity. We believe:
· All people have the right to live to their fullest potential.
· All communities have the right to create environments that allow them to grow and thrive.
· Public health policy must be based on collaboration and true community partnerships.
· Genuine public health progress must be based on the recognition that knowledge comes in many forms and many places in our society.
· Success and progress will only come when we treat people, communities, partners, and staff with care and respect.
Join us!
We are seeking a skilled and dynamic Research Associate with experience conducting research and using evidence for decision-making. Candidates should have experience with designing and analyzing rigorous quantitative and qualitative research and have strong communication and technical writing skills.
The Associate will plan, manage and implement data analytic activities related to the work of the Get Healthy Philly team. This will include collecting, cleaning, and managing data; performing statistical analysis; and summarizing results for scientific, policy-oriented, and public audiences. The Associate will use appropriate data sources to monitor trends, patterns, and changes in risk factors and health outcomes. Factors of interest include the health behaviors of individuals, the demographic characteristics of populations, the policy environment, and the built environment. While academic journal publications are encouraged, the primary purpose of our work is to inform and advise policymakers and the public.
JOB SPECIFICATIONS
Responsibilities/Duties
· Reviews and synthesizes existing literature on topics related to chronic conditions and injury prevention
· Develops and fields data collection efforts, including surveys
· Manages, cleans, analyzes, and interprets data
· Performs regular data matches between health-related data sources
· Guides research projects through Institutional Review Board approval
· Collaborates with academic, medical, and policy partners
· With a team, develops new research and data analysis tasks based on the Division's needs
· Contributes to research and data products including reports, data briefs, charts, presentations, and manuscripts
· Works collaboratively with other Associates and Analysts to develop the analysis skills of the entire team
· Contributes to program evaluation planning
· Contributes to writing grants
· Contributes to manuscript development for peer-reviewed journals
· Participates in division meeting
Qualifications
Qualifications
· A master's degree or PhD in epidemiology, public policy, demography, economics, data science, statistics, or a related field.
· Two to five years of experience in public health or social science research.
· Demonstrated experience in data analysis with statistical software such as R, Stata, or SAS.
OR
· Any equivalent combination of education and experience determined to be acceptable by the Department of Public Health which has included a bachelor's degree as an educational minimum.
Desired skills
· Knowledge of and experience with epidemiological or social science research methods, including study design, methodology, and preparation of scientific reports
· Ability to analyze data, write project proposals, and write technical reports
· Ability to summarize findings for a variety of audiences, e.g. scientists, policy makers, and the public
· Interest in using data skills in an applied setting to advance health policy goals
· Strong analytic abilities with statistical software (e.g., R, Stata, SAS, etc.)
· Experience with interactive data visualization and/or mapping software a plus
· Excellent oral and written communication skills
· Experience working with sensitive health information
· Able to work as a team, prioritize and handle multiple tasks and deadlines, and work independently
Work Environment
Standard office setting with extended periods at work station and periodic use of office equipment.
Position Type and Work Schedule
Full
time position, typical hours are Monday through Friday 8:30 am to 5:00 pm. Flex office schedule options available with supervisor approval.
Travel
Frequent local travel between sites to attend meetings. May occasionally travel outside the city.
Physical Demands
Limited physical demands. Associate will work primarily in an office setting.
Salary and Benefits
Our employees are our most valuable resource, so we offer a competitive and comprehensive benefits package, which can include:
· Medical with vision benefits
· Dental insurance
· Flexible spending accounts
· Life, AD&D and long-term care insurance
· Short- and long-term disability insurance
· 403(b) Retirement Plan, with a company contribution
· Paid time off including vacation, sick, personal and holiday
· Employee Assistance Program
Eligibility and participation are handled consistent with the plan documents and HFP policy.
TO APPLY
To apply, please submit:
1) A resume or CV
2) A cover letter that includes:
a. Your experience with statistical software such as R, SAS or Stata,
b. Your experience in or with Philadelphia, if any, and
c. Your past or proposed contributions to diversity, equity, and inclusion.
3) A writing sample (optional)
Additional Information
All applicants must apply to the position through the following link. Also, please upload a resume and cover letter when applying.
https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=32012&clientkey=703E6F23E139A9E15CD4746A9D25637D&jpt=1b79bf1ead1b4f21088d5e**********
Research Faculty, Center for Sleep & Circadian Rhythms
Winston-Salem, NC jobs
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Research Faculty, Center for Sleep & Circadian Rhythms
Winston Salem, NC, United States
Shift: 1st
Job Type: Regular
Share: mail
Auto-ApplyResearch Associate
Salt Lake City, UT jobs
Job DescriptionSalary: $27 DOE
Research Associate
is part of a team that supports the analytical studies for regulatory submissions of
in vitro
diagnostic (IVD) products developed by BioFire Defense. The primary responsibility is to execute and report on performance studies that demonstrate products and devices are functioning in accordance with design and regulatory requirements and specifications. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to effectively and respectfully communicate and coordinate with peers and supervisors.
Other key skills required:
Knowledge of microbiology and molecular biology principles, tools, and techniques
Knowledge of basic laboratory practices including pipetting, handling of biological and chemical materials, sterile techniques, and contamination control
Knowledge of basic statistical and concentration calculations
Attention to detail, critical thinking, trouble shooting, and problem solving skills
Ability to collaborate in a fast-paced environment
Proficiency with Microsoft Office Suite
May be required to obtain and maintain a DoD Personnel Security Clearance.
Education
Minimum of a bachelors degree with emphasis in a science, or related field.
Experience
Research Associate I Six months experience in an academic, industry, or healthcare laboratory
Research Associate II Two years experience in an academic, industry, or healthcare laboratory in addition to experience with real-time PCR and/or sequence analysis and familiarity with Biosafety Level 2 practices
Benefits:
Medical
Dental
Vision
401k - company match of 5% regardless of participation and up to a total of 9.5% company match if contributing
4 Weeks of PTO
9 Paid Holidays
Paid Winter Break from the work week between December 24 thru December 31
Participation in Company's Wellness Program (discounted medical premiums)
Multiple Company Sponsored Events Each Year (catered breakfast/lunch, holiday parties, snacks)
Stimulating work environment
Convenient location near I-15 and Trax Station
Free Parking
Our EEO Policy
BioFire Defense is an equal opportunity employer (M/F/D/V). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. BioFire Defense complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Research Faculty, Center for Sleep & Circadian Rhythms
Wake Forest, NC jobs
Department:
36621 Wake Forest University Health Sciences - Nursing Psychiatric
Status:
Full time
Benefits Eligible:
Yes
Hours Per Week:
40
Schedule Details/Additional Information:
Monday to Friday, First Shift
Pay Range
$0.00 - $0.00
Wake Forest University School of Medicine and Atrium Health Wake Forest Baptist (AHWFB) are seeking research faculty to join their emerging Center for Sleep & Circadian Rhythms. This is a unique opportunity to join a thriving and rapidly growing medical school and academic health system in a beautiful, vibrant, diverse and affordable community.
The ideal candidate is a scientist or clinician-scientist at the level of Associate Professor or Professor (could be PhD, MD or MD/PhD) with expertise in epidemiology, behavioral sleep medicine, or clinical psychology. The faculty appointment would reside in an individual department based on the primary specialty of the candidate, with relevant joint appointments in related departments to foster interdisciplinary and translational research. If a team will accompany an applicant, departmental recruitments would be discussed with chairs to fund additional faculty.
Center Goals: A main goal of the Center is to develop a nationally-recognized center for sleep and rhythms research, capitalizing on the research strengths at Wake Forest and access to the large population served by the Advocate Health system, with its shared electronic medical record and single IRB. The short-term goals of the Center are to:
Recruit a team of experts with skills that are generalizable across multiple areas of sleep and rhythms research.
Create a centralized resource of sleep and rhythms expertise and technologies for use throughout the Enterprise (both research and clinical domains), and serve as a coordinating ‘hub' for bringing together different investigators and organizational units involved in sleep- and rhythms-related research and clinical practice.
Oversee development of center grants, training grants, and clinical trials related to the study of sleep and rhythms and their disorders.
Pilot new ideas with input from community and organizational partners.
Atrium Health Wake Forest Baptist's sleep center is accredited by the American Academy of Sleep Medicine. It has eight adult and two pediatric sleep beds. In Charlotte, Atrium Health offers the largest comprehensive sleep center in the Carolinas, with 14 sleep testing locations and 25 board certified sleep specialists seeing over 20,000 patient visits annually across the region.
Atrium Health Wake Forest Baptist
Atrium Health Wake Forest Baptist Health (www.WakeHealth.edu) is a nationally recognized academic health system in Winston-Salem, NC, with an integrated enterprise serving 24 counties in NC and Virginia. It comprises a regional clinical system with more than 300 locations, 2,100 physicians and 1,535 acute care beds; Wake Forest School of Medicine; and Wake Forest Innovations, which promotes the commercialization of research discoveries.
This is a time of tremendous growth for Wake Forest. In 2020, Wake Forest Baptist Health and Atrium Health officially joined together as a single enterprise. As part of this new enterprise, Atrium Health announced $3.4 billion in planned investments in our health system and the communities we serve, including the construction of a second full campus of the School of Medicine in Charlotte. The growth of the medical school will expand existing academic research capabilities and opportunities for population health and clinical trials across a large, diverse market.
Advocate Health
Advocate Health is the fifth-largest nonprofit integrated health system in the United States - created from the combination of Advocate Aurora Health and Atrium Health in December 2022. Providing care under the names Advocate Health Care in Illinois, Atrium Health in the Carolinas, Georgia and Alabama, and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care, with Wake Forest University School of Medicine serving as the academic core of the enterprise. Headquartered in Charlotte, North Carolina, Advocate Health serves nearly 6 million patients and is engaged in hundreds of clinical trials and research studies. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs nearly 150,000 team members across 67 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to equitable care for all, Advocate Health provides nearly $5 billion in annual community benefits.
Winston-Salem, North Carolina
Located in Forsyth County (population ≈376,000) in the Piedmont Triad region of NC, Winston-Salem is the state's fifth largest city, featuring a moderate climate with all four seasons and housing costs ≈32% below the national average. Residents enjoy a vibrant restaurant scene, a wide variety of indoor and outdoor recreational opportunities, strong public/private schools, enthusiastic support for the arts, and close proximity to the Appalachian Mountains and Atlantic Coast beaches.
A comprehensive position description is available upon request.
Wake Forest School of Medicine, Atrium Health Wake Forest Baptist, Wake Forest Baptist Medical Center and Advocate Health are Affirmative Action and Equal Opportunity Employers with a strong commitment to achieving diversity among faculty and staff.
Interested candidates may contact:
Thavone Khounthikoumane
Talent Acquisition Program Manager
Wake Forest University School of Medicine
Thavone.Khounthikoumane@Advocatehealth.org
Our Commitment to You:
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more - so you can live fully at and away from work, including:
Compensation
Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance
Benefits and more
Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
About Advocate Health
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.
Auto-ApplyResearch Faculty, Center for Sleep & Circadian Rhythms
Winston-Salem, NC jobs
Department: 36621 Wake Forest University Health Sciences - Nursing Psychiatric Status: Full time Benefits Eligible: Yes Hours Per Week: 40 Schedule Details/Additional Information: Monday to Friday, First Shift Pay Range $0.00 - $0.00 Wake Forest University School of Medicine and Atrium Health Wake Forest Baptist (AHWFB) are seeking research faculty to join their emerging Center for Sleep & Circadian Rhythms. This is a unique opportunity to join a thriving and rapidly growing medical school and academic health system in a beautiful, vibrant, diverse and affordable community.
The ideal candidate is a scientist or clinician-scientist at the level of Associate Professor or Professor (could be PhD, MD or MD/PhD) with expertise in epidemiology, behavioral sleep medicine, or clinical psychology. The faculty appointment would reside in an individual department based on the primary specialty of the candidate, with relevant joint appointments in related departments to foster interdisciplinary and translational research. If a team will accompany an applicant, departmental recruitments would be discussed with chairs to fund additional faculty.
Center Goals: A main goal of the Center is to develop a nationally-recognized center for sleep and rhythms research, capitalizing on the research strengths at Wake Forest and access to the large population served by the Advocate Health system, with its shared electronic medical record and single IRB. The short-term goals of the Center are to:
* Recruit a team of experts with skills that are generalizable across multiple areas of sleep and rhythms research.
* Create a centralized resource of sleep and rhythms expertise and technologies for use throughout the Enterprise (both research and clinical domains), and serve as a coordinating 'hub' for bringing together different investigators and organizational units involved in sleep- and rhythms-related research and clinical practice.
* Oversee development of center grants, training grants, and clinical trials related to the study of sleep and rhythms and their disorders.
* Pilot new ideas with input from community and organizational partners.
Atrium Health Wake Forest Baptist's sleep center is accredited by the American Academy of Sleep Medicine. It has eight adult and two pediatric sleep beds. In Charlotte, Atrium Health offers the largest comprehensive sleep center in the Carolinas, with 14 sleep testing locations and 25 board certified sleep specialists seeing over 20,000 patient visits annually across the region.
Atrium Health Wake Forest Baptist
Atrium Health Wake Forest Baptist Health (www.WakeHealth.edu) is a nationally recognized academic health system in Winston-Salem, NC, with an integrated enterprise serving 24 counties in NC and Virginia. It comprises a regional clinical system with more than 300 locations, 2,100 physicians and 1,535 acute care beds; Wake Forest School of Medicine; and Wake Forest Innovations, which promotes the commercialization of research discoveries.
This is a time of tremendous growth for Wake Forest. In 2020, Wake Forest Baptist Health and Atrium Health officially joined together as a single enterprise. As part of this new enterprise, Atrium Health announced $3.4 billion in planned investments in our health system and the communities we serve, including the construction of a second full campus of the School of Medicine in Charlotte. The growth of the medical school will expand existing academic research capabilities and opportunities for population health and clinical trials across a large, diverse market.
Advocate Health
Advocate Health is the fifth-largest nonprofit integrated health system in the United States - created from the combination of Advocate Aurora Health and Atrium Health in December 2022. Providing care under the names Advocate Health Care in Illinois, Atrium Health in the Carolinas, Georgia and Alabama, and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care, with Wake Forest University School of Medicine serving as the academic core of the enterprise. Headquartered in Charlotte, North Carolina, Advocate Health serves nearly 6 million patients and is engaged in hundreds of clinical trials and research studies. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs nearly 150,000 team members across 67 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to equitable care for all, Advocate Health provides nearly $5 billion in annual community benefits.
Winston-Salem, North Carolina
Located in Forsyth County (population ≈376,000) in the Piedmont Triad region of NC, Winston-Salem is the state's fifth largest city, featuring a moderate climate with all four seasons and housing costs ≈32% below the national average. Residents enjoy a vibrant restaurant scene, a wide variety of indoor and outdoor recreational opportunities, strong public/private schools, enthusiastic support for the arts, and close proximity to the Appalachian Mountains and Atlantic Coast beaches.
A comprehensive position description is available upon request.
Wake Forest School of Medicine, Atrium Health Wake Forest Baptist, Wake Forest Baptist Medical Center and Advocate Health are Affirmative Action and Equal Opportunity Employers with a strong commitment to achieving diversity among faculty and staff.
Interested candidates may contact:
Thavone Khounthikoumane
Talent Acquisition Program Manager
Wake Forest University School of Medicine
Thavone.Khounthikoumane@Advocatehealth.org
Our Commitment to You:
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more - so you can live fully at and away from work, including:
Compensation
* Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
* Premium pay such as shift, on call, and more based on a teammate's job
* Incentive pay for select positions
* Opportunity for annual increases based on performance
Benefits and more
* Paid Time Off programs
* Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
* Flexible Spending Accounts for eligible health care and dependent care expenses
* Family benefits such as adoption assistance and paid parental leave
* Defined contribution retirement plans with employer match and other financial wellness programs
* Educational Assistance Program
About Advocate Health
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.
Research Project Manager
North Chicago, IL jobs
Ann & Robert H. Lurie Children's Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children's Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report.
Location
Simpson Querrey Biomedical Research Center
Job Description
The Research Project Manager will work with Principal Investigator(s) and Research Manager to manage, oversee, and guide ongoing complex research projects to ensure project deliverables and timelines meet expectations. May assist in daily supervisory responsibilities of study/project team members.
Essential Job Functions:
Manages programmatic activities for multiple internally and externally funded, complex research projects, and subsequent activities related to additional and ongoing funding.
Coordinates and manages defined projects consistent with the current, externally funded project plan and future projects.
Oversee operations of ongoing research projects and develops/troubleshoots workflows and processes as needed when challenges arise.
Responsible for pre-award and post-award activities relating to sponsored research grant proposals and projects in conjunction with the Research Business Operations (RBO) offices.
Works with the Research Business Operations (RBO) offices and Office of Clinical and Community Trials (OCCT) to facilitate contract negotiations and execution, to ensure proper accrual tracking, and to provide additional information as needed for timely financial reconciliation, management, and reporting.
Partners with program leaders to develop and oversee relationships with key internal and external stakeholders. This includes working with outside partners (e.g., collaborators, funders, subcontractors, consultants, etc.) and Lurie Children's administrative.
This may include attending all appropriate business meetings, and external meetings, seminars and other activities deemed appropriate in the US and internationally.
Assists with onboarding and training of additional study team members conducting day-to-day activities for ongoing research projects.
Leads the dissemination of research findings through publication preparation, collaboration on abstracts and posters for scientific meetings, presentation of research at national meetings, coordination of presentations at research education conferences, and overseeing the preparation and evaluation of abstracts, posters, and manuscripts.
Contributes to the overall research program leadership through planning, interdisciplinary communication, and collaboration.
Other job functions as assigned.
Knowledge, Skills, and Abilities:
Bachelor's degree with four or more years research experience required. Master's degree and/or relevant research certification preferred.
Excellent organizational skills with ability to manage multiple simultaneous studies.
Excellent verbal and written communications skills. Provides high-quality customer service. Excellent knowledge of FDA, HSR, and GCP Guidelines.
Excellent analytical skills with the ability to understand financial data, recognize quantitative and qualitative research methods.
Remains agile and adaptable plus assists in implementation of various technological systems. Excellent leadership skills with the ability to prioritize tasks, problem solve, and mentor other team members.
Ability to foster an inclusive environment where all team members feel valued and respected.
Education
Bachelor's Degree (Required)
Pay Range
$70,720.00-$115,627.20 Salary
At Lurie Children's, we are committed to competitive and fair compensation aligned with market rates and internal equity, reflecting individual contributions, experience, and expertise. The pay range for this job indicates minimum and maximum targets for the position. Ranges are regularly reviewed to stay aligned with market conditions. In addition to base salary, Lurie Children's offer a comprehensive rewards package that may include differentials for some hourly employees, leadership incentives for select roles, health and retirement benefits, and wellbeing programs. For more details on other compensation, consult your recruiter or click the following link to learn more about our benefits.
Benefit Statement
For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:
Medical, dental and vision insurance
Employer paid group term life and disability
Employer contribution toward Health Savings Account
Flexible Spending Accounts
Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
403(b) with a 5% employer match
Various voluntary benefits:
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Tuition assistance
Student loan servicing and support
Adoption benefits
Backup Childcare and Eldercare
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children's facilities
Discount purchasing program
There's a Place for You with Us
At Lurie Children's, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints - recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care.
Lurie Children's and its affiliates are equal employment opportunity employers. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.
Support email: ***********************************
Auto-ApplyProject Manager II - Research
Salt Lake City, UT jobs
Schedule: Monday - Friday (40 hrs/wk) 8:00 AM - 5:00 PM Department: R&I Innovation - 249 Primary Purpose: The PM-Research supports diagnostic test development, validation, research, and other innovation projects by acting as a central support figure throughout the project lifecycle. This position requires fostering collaboration, documenting progress and ensuring the success of large-scale and complex initiatives. The Project Manager collaborates closely with Scientific Management, scientific staff, and Medical Directors, vendors and external sponsors to ensure scope is communicated and project milestones and deliverables are completed successfully and on schedule. The PM serves as a liaison between technical and non-technical departments to ensure all targets and requirements are met. This position demands a proactive approach to managing projects across various scientific disciplines.
About ARUP:
ARUP Laboratories is a national clinical and anatomic pathology reference laboratory and an enterprise of the University of Utah and its Department of Pathology. Based in Salt Lake City, Utah.
ARUP proudly hires top talent to create a work environment of diversity, professional growth and continuous development. Our workforce is committed to the important service we provide to over one million patients each month. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient's life. We never forget that there is a patient behind every specimen we receive.
We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Consider joining our dynamic team.
Essential Functions:
Manages ARUP research projects, including developing and monitoring project timelines, deliverables, communications, overseeing project scope, and other project requirements.
Supports Scientific Managers, Scientists and Medical Directors as a member of project leadership.
Accountable for organizing project requirements, translating them into defined scope, and ensuring the documentation and communication of project scope are well-maintained.
Creates and executes project charters and other project plan documents and revises as appropriate to meet changing needs and requirements.
Gains a comprehensive technical understanding of the project background.
Communicates risks and issues to stakeholders, including impacts to timelines, and facilitates troubleshooting efforts to address them.
Coordinates project milestones and deliverables to ensure timely completion.
Guide projects from initiation to successful completion, ensuring alignment with organizational goals.
Produces and maintains project dashboards for communication of progress to leadership and project stakeholders.
Understands and ensures adherence to diagnostic test validation policies and procedures, where applicable
Maintains professional relationships with sponsors, stakeholders, team members, vendors, and consultants.
Serves as a liaison between technical and non-technical departments ensuring alignment with targets and requirements.
Act as a central support figure throughout the project lifecycle, focusing on fostering collaboration and ensuring the success of large-scale and complex initiatives.
Collaborates with other departments within ARUP to facilitate test transfer between departments.
Establishes and maintains communication as required with the stakeholders, including leading meetings and hosting stakeholder visits as necessary.
Reviews deliverables prepared by team before passing to client, project sponsor, or stakeholder.
Maintains a comprehensive understanding of project status and uses strong problem-solving, communication and leadership skills to keep projects on track.
Independently or in collaboration with Scientific managers identifies resources needed and assigns responsibilities for a project.
Understands the business challenge proposed by the scientific project team and contributes to resolution.
Analyzes project return on investment, profitability, revenue, and utilization using Business Value Models (BVMs).
Manages project budget, including creating the budget, tracking expenses, and invoicing, as needed.
Follows project management methodologies as defined and outlined by Project Management Institute (PMI) and ARUP policies and procedures.
Manages day-to-day operational aspects of projects and their scope.
Minimizes exposure and risk on project.
Works with minimal oversight from Manager, and mentors junior Project Managers and other supporting team members.
Independently identifies project management requirements.
Oversees project management for an entire project portfolio.
Thorough understanding of ARUP test validation policies and procedures and ensures implementation for relevant projects.
Other duties as assigned.
Physical and Other Requirements:
Stooping: Bending body downward and forward by bending spine at the waist.
Reaching: Extending hand(s) and arm(s) in any direction.
Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc.
Communicate: Frequently communicate with others.
PPE: Biohazard laboratory environment that requires use of personal protective equipment in accordance with CDC and OSHA regulations and company policies.
ARUP Policies and Procedures: To conduct self in compliance with all ARUP Policies and Procedures.
Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects.
Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling.
Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance.
Project Manager Research
Chicago, IL jobs
Ann & Robert H. Lurie Children's Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children's Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report.
Location
Outpatient Services at 1440 N Dayton
Job Description
The Research Project Manager will work with Principal Investigator(s) and Research Manager to manage, oversee, and guide ongoing complex research projects to ensure project deliverables and timelines meet expectations. May assist in daily supervisory responsibilities of study/project team members.
Essential Job Functions:
Manages programmatic activities for multiple internally and externally funded, complex research projects, and subsequent activities related to additional and ongoing funding.
Coordinates and manages defined projects consistent with the current, externally funded project plan and future projects.
Oversee operations of ongoing research projects and develops/troubleshoots workflows and processes as needed when challenges arise.
Responsible for pre-award and post-award activities relating to sponsored research grant proposals and projects in conjunction with the Research Business Operations (RBO) offices.
Works with the Research Business Operations (RBO) offices and Office of Clinical and Community Trials (OCCT) to facilitate contract negotiations and execution, to ensure proper accrual tracking, and to provide additional information as needed for timely financial reconciliation, management, and reporting.
Partners with program leaders to develop and oversee relationships with key internal and external stakeholders. This includes working with outside partners (e.g., collaborators, funders, subcontractors, consultants, etc.) and Lurie Children's administrative.
This may include attending all appropriate business meetings, and external meetings, seminars and other activities deemed appropriate in the US and internationally.
Assists with onboarding and training of additional study team members conducting day-to-day activities for ongoing research projects.
Leads the dissemination of research findings through publication preparation, collaboration on abstracts and posters for scientific meetings, presentation of research at national meetings, coordination of presentations at research education conferences, and overseeing the preparation and evaluation of abstracts, posters, and manuscripts.
Contributes to the overall research program leadership through planning, interdisciplinary communication, and collaboration.
Other job functions as assigned.
Knowledge, Skills, and Abilities:
Bachelor's degree with four or more years research experience required. Master's degree and/or relevant research certification preferred.
Excellent organizational skills with ability to manage multiple simultaneous studies.
Excellent verbal and written communications skills. Provides high-quality customer service. Excellent knowledge of FDA, HSR, and GCP Guidelines.
Excellent analytical skills with the ability to understand financial data, recognize quantitative and qualitative research methods.
Remains agile and adaptable plus assists in implementation of various technological systems. Excellent leadership skills with the ability to prioritize tasks, problem solve, and mentor other team members.
Ability to foster an inclusive environment where all team members feel valued and respected.
Education
Bachelor's Degree (Required)
Pay Range
$70,720.00-$115,627.20 Salary
At Lurie Children's, we are committed to competitive and fair compensation aligned with market rates and internal equity, reflecting individual contributions, experience, and expertise. The pay range for this job indicates minimum and maximum targets for the position. Ranges are regularly reviewed to stay aligned with market conditions. In addition to base salary, Lurie Children's offer a comprehensive rewards package that may include differentials for some hourly employees, leadership incentives for select roles, health and retirement benefits, and wellbeing programs. For more details on other compensation, consult your recruiter or click the following link to learn more about our benefits.
Benefit Statement
For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:
Medical, dental and vision insurance
Employer paid group term life and disability
Employer contribution toward Health Savings Account
Flexible Spending Accounts
Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
403(b) with a 5% employer match
Various voluntary benefits:
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Tuition assistance
Student loan servicing and support
Adoption benefits
Backup Childcare and Eldercare
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children's facilities
Discount purchasing program
There's a Place for You with Us
At Lurie Children's, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints - recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care.
Lurie Children's and its affiliates are equal employment opportunity employers. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.
Support email: ***********************************
Auto-Apply