Oncology RWE/Epi Scientist
Scientist job in Pearl River, NY
Senior Manager, MED RWE/Epi Scientist
The Senior Manager, RWE/Epi Scientist, position within Medical Evidence Development (MED) Real-World Evidence & Epidemiology (RWE/Epi) provides an opportunity for a collaborative epidemiologist to support real-world evidence and epidemiologic studies as part of Medical strategy across the entire drug development process. The candidate will be responsible for synthesizing the literature and contributing to the design, conduct and reporting of global epidemiologic research studies on Pfizer I&I products. The Senior Manager will also be accountable for the quality, timeliness, and efficiency of all RWE/Epi deliverables in assigned product/disease area, and maintain an internal network of Pfizer stakeholders to cultivate innovation, cross-functional collaboration, and identify new opportunities for RWE/Epito increase the value of Pfizer assets. The candidate will develop external partnerships to leverage data resources and collaboration on high priority global studies. Responsibilities include authoring and reviewing study protocols, reports, and presentations, as well as communication in writing and presentations to internal stakeholders, regulatory authorities, and medical professionals. The candidate will also be responsible for non-study deliverables such as RWE insights, epidemiology literature reviews, regulatory responses, and department initiatives.
This position will report directly to the Hem-Onc Team Lead in RWE/Epi.
Capabilities
Skill and experience identifying, designing and supporting or leading real-world evidence studies of disease epidemiology and effectiveness as part of the global cross-functional Integrated Evidence Plan.
Maintain knowledge and awareness of internal and external data resources and identify appropriate studies for addressing questions of interest, recognizing the limitations and strengths of various design options and data sources
Partner with Chief Medical Office colleagues to address asset team evidence needs and support global regulatory submissions to the FDA, EMA and other agencies.
Deliver rapid insights from real-world, observational data source
Develop and deliver presentations, webinars, manuscripts, scientific data packages or other communication modalities
Assure the highest standards of quality, compliance and management of all research activities
Participate in RWE/Epi peer review of study protocols and study reports
Document all requests and track progress toward project completion, other metrics and business goals
Qualifications
PhD in Epidemiology, Statistics/Biostatistics, Health Outcomes Research, Quantitative Methods, Public Health, Health Economics, or Other Biological Science fields with a substantial quantitative component and at least 1 years of relevant experience in the pharmaceutical, academic and/or medical environment; or, MPH or another relevant Master's degree and at least 5 years of experience in the pharmaceutical, academic and/or medical environment, at least 1 of which were in the pharmaceutical industry.
Demonstrated strong quantitative skills and methods expertise to generate rapid insights from real-world / observational data source
Demonstrated strong technical writing skills and oral presentation skills with a track-record of publishing in peer-reviewed journals and presenting at medical/scientific conferences
Demonstrated ability to convert complex analysis into meaningful insights with data visualization and presentation tools and able to manipulate and analyze complex structured and unstructured data from multiple real world evidence sources.
Ability to work under pressure with a high level of autonomy/leadership on research projects and collaborate with multiple partners in a matrixed environment
Knowledgeable of the external regulatory environment for real-world evidence and maintains awareness of scientific developments in epidemiology, medicine, and technology (e.g., artificial intelligence).
Bonus Points If You Have (Preferred Requirements):
Proficiency in rapid real-world data analytical platforms
Experience working with real-world data (RWD) including Electronic Medical Records (EMR), claims, and surveys
Excellent problem-solving and decision-making abilities
Ability to influence and collaborate with senior management and stakeholders
Strong project management skills with the ability to handle multiple projects simultaneously
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
PHYSICAL/MENTAL REQUIREMENTS
Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis.
Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.
OTHER JOB DETAILS
Last Date to Apply for Job: December 29, 2025
Eligible for Relocation Package: No
The annual base salary for this position ranges from $135,100.00 to $225,100.00.* In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.* The annual base salary for this position in Tampa, FL ranges from $121,600.00 to $202,600.00.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make ********************** accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email ...@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Medical
Clinical Laboratory Scientist
Scientist job in White Plains, NY
Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Himanshi Pandits at email address ****************************** can be reached on # ************.
We have Permanent Role of Clinical Laboratory Scientist for our client at White Plains, NY Please let me know if you or any of your friends would be interested in this position
Position Details:
Clinical Laboratory Scientist, White Plains, NY
Location : White Plains, NY 10601
Project Duration : Full Time/Permanent
Shift Timing : Mon-Fri 8am-4pm rotating w/e and hol
Salary : $93,873.00 - $120,685.50
Position Summary
The Clinical Laboratory Scientist performs laboratory testing using both manual and automated techniques. Performs other duties as assigned.
Essential Functions and Responsibilities Includes the Following:
Understands and adheres to the WPH performance standards, policies, and behaviors
Laboratory testing personnel responsibilities include:
Following the laboratory's pre-analytic and analytic procedures and maintaining records of these tests
Maintaining records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens
Adhering to the laboratory's quality assurance procedures, including documenting all:
Quality control activities including quality control testing and calibrations
Instrument and equipment verifications
Maintenance and preventative maintenance
Following the laboratory's policies and procedures whenever test systems are not within the laboratory's established performance specifications
Identifying and documenting problems that may adversely affect test performance and notifying the supervisor, assistant director or director and documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications
Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing.
Notifies and documents clinicians and patient units of all critical values and maintains the laboratory STAT turn around time requirements.
Participates in regulatory readiness for CAP, AABB, NYSDOH, and Joint Commission.
Maintains 12 Continuing Education credits per year.
Understands and participates in standard operating procedures, proficiency testing, inspection audits, quality program including reporting non-conformances.
Evaluates test results for abnormalities and confirms those results per department protocols where required.
Participates in validations, training, and competency assessments as required.
Responsible for inventory management of lot numbers, expiration dates, labeling, and QC requirement.
Completes all annual mandatory training, in-services, and ongoing education as required.
Performs other duties as assigned.
Section testing training and competency assessments are maintained by the section laboratory supervisor for all assigned disciplines
Sections are listed below:
Generalists - performs Hematology, Coagulation, Chemistry/Immunology, Urinalysis, Microbiology, and Blood Bank specialties
Chemistry/Immunology - Performs Chemistry, Specialized Chemistry, Immunology, Molecular, and Serology testing
Hematology - Performs Hematology, Coagulation, and Urinalysis testing
Microbiology - Performs Bacteriology, Parasitology, Virology, Mycology, Mycobacteriology, Susceptibilities, and Molecular testing
Blood Bank - Performs blood bank testing related to transfusion medicine and blood product distribution.
Anatomic Pathology - Performs histological procedures for routine, specials stains, and immunohistochemistry
Education & Experience Requirements :
Current NYS License as a Clinical Laboratory Technologist required.
Education in accordance with the NYS Office of Professions and CLIA requirements of testing personnel.
Preferred with ASCP Certification.
Scientist II
Scientist job in Ridgefield, CT
· Operate and maintain flow cytometry instrumentation, including multi-laser cell sorters: · Perform instrument quality control procedures, and oversee instrument performance on a daily basis. · Perform preventive maintenance on cytometry instrumentation and equipment in the laboratory.
· Troubleshoot instrument malfunctions and coordinate service repairs with field service engineers, as needed.
· Perform cell sorting to support Research projects.
· Provide technical support on instrument setup and use, experiment design, and data analysis to instrument Users.
· Develop and maintain policies for Cytometry Core Facility.
· Develop cytometry applications to support Research projects, as needed.
Skills:
· Previous experience working in a flow cytometry core facility preferred.
· Has worked with Client cytometry instrumentation. Excellent communication, customer service, and interpersonal skills.
· Mechanical and technical expertise. Experience developing and executing polychromatic flow cytometry panels.
· Expertise in flow cytometry data analysis including, but not limited to FACS Diva software, and FlowJo.
· Experience operating various cell sorters preferred.
· Education: Bachelors Degree
Additional Information
All your information will be kept confidential according to EEO guidelines.
Bench Scientist
Scientist job in New Haven, CT
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Job Description
•Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed.
•Performed general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software.
•Performed quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques.
•Operated, maintained, calibrated and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs.
•Maintained quality control and calibration logs of all Flow Cytometers.
•Analyzed, summarized and document experimental results.
•Performed data entry using laboratory information management system (LIMS)
•Write experimental SOPs.
•Update Biomarker Lead on the status, results and problems in method development and performance of the assays.
•Complete all NHCRU/Pfizer required training.
•Have a working knowledge of Microsoft office including Excel, Word and PowerPoint.
•Possess multi-tasking and organizational skills.
•Experience in ELISpot Assays and FlowJo software a plus.
Qualifications
MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience
BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience.
Additional Information
To schedule interview or get any further information feel free to contact:
Sagar Rathore
************
******************************
Easy ApplyScientist II
Scientist job in Ridgefield, CT
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Title: Scientist II
Location: Ridgefield Main Campus, 900 Ridgebury Road - R&D, Ridgefield, CT
Duration: 2 year
Duties:
As a biomarker scientist, you will work with animal and human samples to identify, develop and validate novel biomarkers of kidney pathology and therapy. The biomarker assays will involve work with protein, RNA, and exosomes from tissue, urine, blood and require extensive knowledge, good lab skills and strong data analysis capability.
Identify, develop, and validate novel biomarkers based on project needs.
Develop and establish new biomarker assays.
Perform general biomarkers assays and analyze the data.
Clearly communicate timelines and study results within the group and with project teams.
Skills:
Requirements:
Experience working in a lab to perform routine lab experiments (Cell culture, sample preparation, ELISA, Western blot, qRTPCR, etc.)
Independently and /or collaboratively performs scientific experiments (in vitro, in vivo and ex vivo) with a predefined goal including developing new methodologies, protocols and/or testing procedures that contribute to project /research goals.
Trouble-shooting skills during assay development and optimization
Strong communication skills.
Desired Experience, Skills and Abilities:
Experience with biomarker assay technologies including antibody-based detection methods (e.g. ELISA) and multiplexed detection methods (e.g. Luminex, MSD) is desired.
Hands-on experience in the development and validation of biomarker assays in the preclinical and clinical setting is desired.
A proven track record of research accountability and productivity within a team setting is highly desired.
The successful candidate will be a self-motivated, accountable bench scientist with the ability to apply his/her skills to meet diverse project needs in a fast-paced dynamic team environment.
Qualifications
Education:
Bachelor's Degree in relevant scientific discipline (e.g. cell biology, molecular biology, biochemistry, etc.); Master's degree is highly preferred.
Additional Information
Thanks & Regards,
Debasis Banerjee
201 - 613 - 5158
debasis@ustechsolutionsinc(dot)com
R&D Scientist
Scientist job in Valhalla, NY
A global leader in food and beverage is interviewing for a contract Research and Development Scientist position in Valhalla, NY. The incumbent will conduct and support ingredient application programs.
Qualifications:
BS/MS Food Science & Technology / Food Chemistry or related field
• 3-5 years of experience in the Food Industry or related area
• Understanding of food chemistry, carbohydrates, product formulation and development, ingredient technology, and food safety
• Functional knowledge of analytical test methodologies and data interpretation
• Ability to make significant technical, and scientific advances utilizing internal and/or external resources.
• Detail-oriented individual with proven ability to independently lead multiple projects and work streams simultaneously, leveraging project management tools.
• Self-starter with good oral and written communication and presentation skills, the ability to work with various personalities and work styles,
• Ability to travel when needed
Biology Scientists (In Vivo)
Scientist job in Pearl River, NY
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description:
• scientist in the cancer in vivo pharmacology group with in vivo experience in small mammals (mouse/rats-preference in immune compromised strains) to support a team of in vivo pharmacologists execute in vivo tumor biology studies both within the vivarium and research lab.
• The candidate must function as an integral member of the in vivo biology team, responsible for supporting all assigned aspects of in vivo testing in a coordinated manner with other members of the team.
• The candidate must be dependable and possess excellent time management, communication, and organizational skills.
Qualifications
Mouse handling (preferable immune deficient), dependability, teamwork, sterile technique, tissue culture, and lab maintenance.
Additional Information
Best Regards,
Anuj Mehta
************
Biology Scientist
Scientist job in Pearl River, NY
Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.
To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com
Job Description
The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX work at Pfizer.
Scope of work
• The contingent worker will be responsible for mouse cancer model development.
• This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts.
• This work requires sterile technique and attention to detail
• Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).
• The worker will also be required to participate in all of the preparation steps necessary for animal studies: surgical tool preparation, tool sterilization, and animal shaving and preparation.
Qualifications
Required skills / background
• The worker should have a minimum 1-3 years' experience working with mice, preferably immune deficient mice.
• The workers should also have experience in small animal surgery and sterile techniques.
• The workers should preferably have knowledge of cancer research experimental designs and methods. Experience with dosing mice would be useful but is not a strict requirement.
Additional Skills:
• What are the most critical skills needed? Mouse handling (preferable immune deficient), mouse surgery, sterile technique, tissue culture, and database maintenance
• What level candidate are you seeking? (i.e. 1-3yrs = Base/Entry; 4-7yrs = Intermediate; 7+ = Advanced)
• Entry or intermediate dependent upon experience and skill sets
Additional Information
All your information will be kept confidential according to EEO guidelines.
IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-573-4748 ASAP!
I look forward to hearing from you!
Biology Scientists (In Vivo)
Scientist job in Pearl River, NY
Makro Scientific:
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX.The workers should also have experience in small animal surgery and sterile techniques.The workers should preferably have knowledge of cancer research experimental designs and methods.Experience with dosing mice would be useful but is not a strict requirement
Qualifications
B.S. degree in Biology, The worker should have a minimum 1-3 years' experience in small animal surgery and sterile techniques working with mice, preferably immune deficient mice.
Additional Information
The responsible for mouse cancer model development.This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts.This work requires sterile technique and attention to detail.Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).
Clinical Research Scientist - Breast Cancer Franchise
Scientist job in Stamford, CT
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Position Overview:
The Development Clinical Research Scientist (CRS) in the Breast Cancer Franchise will be primarily focused on late phase assets in an evolving portfolio. This role is pivotal in the design, execution, and analysis of clinical trials that support the development of innovative breast cancer therapies. The CRS ensures that all medical team activities align with the medical vision and comply with current regulations, laws, guidance (e.g. FDA, ICH, and CPMP etc.), Good Clinical Practices (GCPs), company standards, and Lilly policies.
This position requires close collaboration with cross-functional partners including medical affairs, clinical operations, regulatory, statistics and data science to advance the oncology pipeline and improve patient outcomes. The successful candidate will proactively identify, assess, and mitigate risks related to medical oversight of clinical trials and contribute to regulatory submissions, external engagements, and data disclosure activities.
This role includes supervisory responsibilities and requires demonstrated leadership in clinical development, strong mentoring capabilities, and exceptional written communication skills-particularly for external data disclosures and regulatory documentation.
Primary Responsibilities
* Contribute to the development and execution of clinical strategies for breast cancer programs. Maintain a focus on accelerating timelines while ensuring quality.
* Demonstrate compliance with procedures and be accountable for compliance of team members.
* Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports.
* Supervise and participate in medical monitoring activities, including data review, safety assessments, and protocol deviation management.
* Collaborate with Global Medical Leads, statisticians, and clinical operations to ensure scientific integrity and operational excellence.
* Collaborate with Global Patient Safety on risk management planning.
* Serve as a resource for sites, monitors, investigators, and ethics committees to address study-related questions.
* Provide scientific input for site selection, investigator meetings, steering committees, and clinical trial training.
* Participate in data analysis, scientific dissemination, and preparation of final study reports.
* Analyze and contextualize clinical data to support decision-making and portfolio strategy.
* Contribute to strategic planning and innovation through cross-functional working groups.
* Support planning and execution of symposia, advisory boards, and other external engagements.
* Develop and review scientific materials including slide decks, abstracts, posters, and manuscripts.
* Support regulatory submissions (e.g., INDs, NDAs, BLAs) and prepare materials for health authority interactions.
Scientific & Technical Expertise and Development
* Stay current with medical literature and scientific developments in breast oncology.
* Maintain deep knowledge of clinical practice trends, access considerations, and relevant preclinical and clinical data.
* Provide scientific consultation to medical affairs, health outcomes, and commercial teams.
* Assist in planning and execution of opportunities for external scientific engagement and attend relevant symposia.
Leadership & Professional Development
* Model leadership behaviors and lead matrixed, cross-functional teams. Direct supervision of a team of more junior scientists.
* Set and help members of the team pursue developmental goals though coaching to drive exceptional team performance while elevating the individual.
Basic qualifications:
* PhD with 3+ years of industry experience) OR (BS Degree or equivalent experience in Health-related field with 10+ years' industry experience
* 3+ years of clinical research scientist experience/clinical trial experience
* Direct Line Leadership experience
Additional Information/Preferences:
* Breast cancer disease state knowledge/experience
* An advanced health/medical/scientific graduate degree such as, PharmD, PhD, MSN with advanced clinical specialty (Clinical Nurse Specialist/Nurse Practitioner)
* Experience with all phases of a trial lifecycle: design, study start up, implementation, and regulatory submission.
* Proven strong communication, interpersonal, teamwork, organizational, and negotiation skills
* Demonstrated ability to influence others (both cross-functionally and within the function) to build a positive working environment.
* Ability to engage in domestic and international travel to the degree appropriate to support the business of the team.
* Fluent in English, verbal and written communication
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$177,000 - $308,000
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Auto-ApplyEmbryologist- Level II
Scientist job in Norwalk, CT
Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice.
The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience.
This is a full-time position working daytime hours with weekend and holiday rotations.
Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person.
At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
Benefits:
401(k)
401(k) matching
Dental insurance
Employee assistance program
Employee discount
Flexible spending account
Health insurance
Life insurance
Paid time off
Referral program
Tuition reimbursement
Vision insurance
Schedule:
Holidays
Monday to Friday
Weekend availability
Ability to commute/relocate:
Norwalk, CT 06851
Experience:
Embryology: 2 year
Work Location: In person in Norwalk, CT
Auto-ApplyEmbryologist- Level II
Scientist job in Norwalk, CT
Job Description
Enjoy what you do while contributing to a company that makes a difference in people's lives. Illume Fertility seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice.
The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. We currently have openings for a full-time Embryologists from Entry level through Senior Level to work in our fast paced, high volume, Embryology Lab located at Norwalk, CT office. Level and salary is directly related to the candidate's experience.
This is a full-time position working daytime hours with weekend and holiday rotations.
Skills & Requirements: BS/MS in biologic science required; MT certification considered. Training provided but embryology and/or laboratory experience such as cell culture experience preferred. Must be able to work cooperatively with a multidisciplinary team to provide excellent patient care. More important than the best skills, however, is the right person.
At Illume Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team!
Benefits:
401(k)
401(k) matching
Dental insurance
Employee assistance program
Employee discount
Flexible spending account
Health insurance
Life insurance
Paid time off
Referral program
Tuition reimbursement
Vision insurance
Schedule:
Holidays
Monday to Friday
Weekend availability
Ability to commute/relocate:
Norwalk, CT 06851
Experience:
Embryology: 2 year
Work Location: In person in Norwalk, CT
Biomarker Scientist
Scientist job in New Haven, CT
Primary Responsibilities: Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed. Perform general flow cytometry operation, including sample preparation and analysis.
Experience in FACSCanto Flow Cytometer and FACSDiva software.
Perform quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques.
Operate, maintain, calibrate and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs.
Maintain quality control and calibration logs of all Flow Cytometers.
Analyze, summarize and document experimental results.
Perform data entry using laboratory information management system (LIMS)
Write experimental SOPs.
Update Biomarker Lead on the status, results and problems in method development and performance of the assays.
Complete all NHCRU/Client required training.
Have a working knowledge of Microsoft office including Excel, Word and PowerPoint.
Possess multi-tasking and organizational skills.
Experience in ELISpot Assays and FlowJo software a plus.
Qualifications:
Minimum of either
MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience
BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Bench Scientist
Scientist job in New Haven, CT
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Job Description
•Assist Lead Biomarker Scientist to develop, optimize, validate, and perform FACS-based and other biomarker assays to support studies in New Haven CRU and external protocols if needed.
•Performed general flow cytometry operation, including sample preparation and analysis. Experience in FACSCanto Flow Cytometer and FACSDiva software.
•Performed quality control checks on Flow Cytometers and other Laboratory instruments, reagents, and techniques.
•Operated, maintained, calibrated and trouble shoot Flow cytometers and other Laboratory instruments according to SOPs.
•Maintained quality control and calibration logs of all Flow Cytometers.
•Analyzed, summarized and document experimental results.
•Performed data entry using laboratory information management system (LIMS)
•Write experimental SOPs.
•Update Biomarker Lead on the status, results and problems in method development and performance of the assays.
•Complete all NHCRU/Pfizer required training.
•Have a working knowledge of Microsoft office including Excel, Word and PowerPoint.
•Possess multi-tasking and organizational skills.
•Experience in ELISpot Assays and FlowJo software a plus.
Qualifications
MS in Biology/BioChemistry/Medical Technology plus 1 year of relevant experience
BS in Biology/BioChemistry/Medical Technology or 3 years of relevant experience.
Additional Information
To schedule interview or get any further information feel free to contact:
Sagar Rathore
************
******************************
Easy ApplyScientist IV
Scientist job in Ridgefield, CT
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Duties:
Perform dose formulation analysis under FDA GLPs for nonclinical studies.
Provide dose formulation stability testing for GLP studies.
Develop and validated analytical methods for doser formulation analysis.
Assume responsibility for analytical support of nonclinical studies as contributing scientist/principal investigator working with BI nonclinical drug safety study directors and CRO scientists/study directors.
Review laboratory notebooks and chromatographic data.
Write analytical reports for inclusion in nonclinical study reports.
Write dose formulation stability reports for GLP study support.
Skills:
Expertise in HPLC and analytical method development. Preferred experience in GLPs, Microsoft Office, Empower chromatographic data system.
Qualifications
Education:
Bachelor's Degree and 7-10 years' experience in analytical chemistry/chromatography
Additional Information
Richha Saini
Senior Clinical/Pharmaceutical Recruiter
Tel: ************** Ext 7179
Direct: ************
Biology Scientists (In Vivo)
Scientist job in Pearl River, NY
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
One year position for scientist in the
cancer in vivo pharmacology
group with in vivo experience in small mammals (mouse/rats-preference in immune compromised strains) to support a team of in vivo pharmacologists execute i
n vivo tumor biology studies
both within the vivarium and research lab.
The candidate must function as an integral member of the in vivo biology team, responsible for supporting all assigned aspects of
in vivo testing
in a coordinated manner with other members of the team.
The candidate must be dependable and possess excellent time management, communication, and organizational skills.
Critical Skills:
Mouse handling (preferable immune deficient), dependability, teamwork, sterile technique, tissue culture, and lab maintenance.
Qualifications
Minimum BS degree is required.
Additional Information
Sneha Shrivastava
Technical Recruiter (Clinical/Scientific)
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: ************ | Fax: ************
Connect with us on - LinkedIn | Facebook | Twitter
Biology Scientist
Scientist job in Pearl River, NY
Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.
To find out more about Real Staffing Group please visit
http://www.RealStaffingGroup.com
Job Description
The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX work at Pfizer.
Scope of work
• The contingent worker will be responsible for mouse cancer model development.
• This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts.
• This work requires sterile technique and attention to detail
• Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).
• The worker will also be required to participate in all of the preparation steps necessary for animal studies: surgical tool preparation, tool sterilization, and animal shaving and preparation.
Qualifications
Required skills / background
• The worker should have a minimum 1-3 years' experience working with mice, preferably immune deficient mice.
• The workers should also have experience in small animal surgery and sterile techniques.
• The workers should preferably have knowledge of cancer research experimental designs and methods. Experience with dosing mice would be useful but is not a strict requirement.
Additional Skills:
• What are the most critical skills needed? Mouse handling (preferable immune deficient), mouse surgery, sterile technique, tissue culture, and database maintenance
• What level candidate are you seeking? (i.e. 1-3yrs = Base/Entry; 4-7yrs = Intermediate; 7+ = Advanced)
• Entry or intermediate dependent upon experience and skill sets
Additional Information
All your information will be kept confidential according to EEO guidelines.
IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-573-4748 ASAP!
I look forward to hearing from you!
Biology Scientists (In Vivo)
Scientist job in Pearl River, NY
Makro Scientific: Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations.
Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent.
Job Description
The contingent worker will be working under the supervision of
Oncology In Vivo
Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and
SOPs for PDX
.
The workers should also have experience in small animal surgery and sterile techniques.
The workers should preferably have knowledge of cancer research experimental designs and methods.
Experience with dosing mice would be useful but is not a strict requirement
Qualifications
B.S. degree in Biology, The worker should have a minimum 1-3 years' experience in
small animal surgery and sterile techniques working with mice
, preferably immune deficient mice.
Additional Information
The responsible for mouse cancer model development.
This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts.
This work requires sterile technique and attention to detail.
Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).
Scientist II
Scientist job in Ridgefield, CT
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Title: Scientist II
Location: Ridgefield Main Campus, 900 Ridgebury Road - R&D, Ridgefield, CT
Duration: 2 year
Duties:
As a biomarker scientist, you will work with animal and human samples to identify, develop and validate novel biomarkers of kidney pathology and therapy. The biomarker assays will involve work with protein, RNA, and exosomes from tissue, urine, blood and require extensive knowledge, good lab skills and strong data analysis capability.
Identify, develop, and validate novel biomarkers based on project needs.
Develop and establish new biomarker assays.
Perform general biomarkers assays and analyze the data.
Clearly communicate timelines and study results within the group and with project teams.
Skills:
Requirements:
Experience working in a lab to perform routine lab experiments (Cell culture, sample preparation, ELISA, Western blot, qRTPCR, etc.)
Independently and /or collaboratively performs scientific experiments (in vitro, in vivo and ex vivo) with a predefined goal including developing new methodologies, protocols and/or testing procedures that contribute to project /research goals.
Trouble-shooting skills during assay development and optimization
Strong communication skills.
Desired Experience, Skills and Abilities:
Experience with biomarker assay technologies including antibody-based detection methods (e.g. ELISA) and multiplexed detection methods (e.g. Luminex, MSD) is desired.
Hands-on experience in the development and validation of biomarker assays in the preclinical and clinical setting is desired.
A proven track record of research accountability and productivity within a team setting is highly desired.
The successful candidate will be a self-motivated, accountable bench scientist with the ability to apply his/her skills to meet diverse project needs in a fast-paced dynamic team environment.
Qualifications
Education:
Bachelor's Degree in relevant scientific discipline (e.g. cell biology, molecular biology, biochemistry, etc.); Master's degree is highly preferred.
Additional Information
Thanks & Regards,
Debasis Banerjee
201 - 613 - 5158
debasis@ustechsolutionsinc(dot)com
Biology Scientists (In Vivo) : 2654-1
Scientist job in Pearl River, NY
At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization.
Job Description
The contingent worker will be working under the supervision of Oncology In Vivo Pharmacologists and will be required to adhere to the relevant established Animal Use Protocols and SOPs for PDX work at Pharmaceutical.
Scope of work The contingent worker will be responsible for mouse cancer model development.
This work will primarily be the establishment and maintenance of patient-derived cancer xenografts but could also include development of cell line xenografts.
This work requires sterile technique and attention to detail.
Work is conducted both in an animal facility (vivarium) as well as in biosafety cabinets (laminar flow hoods).
The worker will also be required to participate in all of the preparation steps necessary for animal studies: surgical tool preparation, tool sterilization, and animal shaving and preparation.
Required skills / background -
The worker should have a minimum 1-3 years experience working with mice, preferably immune deficient mice.
The workers should also have experience in small animal surgery and sterile techniques.
The workers should preferably have knowledge of cancer research experimental designs and methods.
Experience with dosing mice would be useful but is not a strict requirement.
Additional Skills:
Mouse handling (preferable immune deficient), mouse surgery, sterile technique, tissue culture, and database maintenance
Level candidate we are seeking (i.e. 1-3yrs = Base/Entry; 4-7yrs = Intermediate; 7+ = Advanced) Entry or intermediate dependent upon experience and skill sets
Qualifications
BS
Additional Information
Best Regards,
Akriti Gupta
**************
Morristown, NJ 07960