Research Associate jobs in National City, CA

We are seeking a highly motivated and qualified individual to join our Discovery Biology Department as a Senior Scientist I and work as part of a team to drive success. The Senior Scientist I will support ongoing RNA-based drug discovery projects in several therapeutic areas. The successful candidate will have experience in neuroscience drug discovery and a deep understanding of human neurobiological processes that drive CNS disease pathophysiology. The Senior Scientist I will employ a variety of in vivo, ex vivo, and in vitro techniques to advance oligonucleotide therapeutics for CNS indications. Essential Responsibilities: Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner. Support the establishment and maintenance of primary and IPSC-derived neuronal cell models. Support in vivo studies by performing basic animal handling and specialized CNS techniques (e.g. intracerebroventricular and intrathecal injection) Perform brain and spinal cord dissections and tissue processing. Collect bodily fluids, e.g. blood and cerebrospinal fluid. Implement multiple state-of-the-art techniques in molecular biology, biochemistry, and microscopy to determine drug distribution, efficacy, safety, and mechanism of action. Critically evaluate, interpret, summarize, and present data to internal project teams and leadership. Maintain a current knowledge of relevant literature, competitive landscape, and methodologies specific to oligonucleotide-based therapeutics targeting CNS disorders. Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audience. Maintain updated and well-organized lab notebooks. Establish and maintain excellent working relationships with critical collaborative partners throughout the company. Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams to carry out assignments. Maintain all appropriate corporate standards for facility safety and hazardous material management. Other duties as assigned. Essential Physical Characteristics: Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: Ph.D. in Neuroscience, Pharmacology, or related scientific discipline 3+ years post-doctoral or biotech/pharmaceutical industry experience in neuroscience research and drug discovery. In-depth knowledge in the field of neuroscience, CNS disease and therapeutic modalities. Expertise in the rodent stereotaxic surgery techniques including intracerebroventricular and intrathecal injection Expertise in rodent brain and spinal cord dissection. Experience with tissue processing, embedding and microtomy of brain tissues, fixation and immunohistochemistry. Experience in gene expression analysis using qPCR and protein analysis techniques. Broad knowledge of scientific experience with track record of scientific achievement demonstrated by peer-reviewed publications. Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders. Strong problem-solving skills and a proactive attitude towards exploring new approaches. Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role. Ability to work as part of a team with a drive to partner effectively with internal and external leaders. Proficiency working with Microsoft Office Suite Products. Preferred Qualifications: Experience with oligonucleotide-based therapeutics is highly desirable. Prior experience in biotech/pharmaceutical industry a plus. Experience in primary neuronal cell cultures and human iPSC-derived neural cells is a plus. Experience in collection of cerebrospinal fluid samples is a plus. Specific experience in fluorescence microscopy and image analysis is desirable. Required Key Attributes: Must be able to work independently as well in cross-functional team settings with supervision as needed. Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism. Self-motivated with excellent interpersonal, organizational and communication skills with the ability to take a hands-on approach to work effectively in a dynamic and collaborative, fast-paced environment. Compensation: This is a full-time position, Monday-Friday, occasional overtime. Pay is commensurate with experience. Equity-based compensation Performance-based bonuses 401(k) with Company Match Medical, Dental, Vision Flexible Spending Account Life Insurance Employee Assistance Program Employee Discounts Paid Vacation Paid Holidays Paid Sick, Jury Duty, Bereavement Work Authorization: United States (Required) Background Check Company Overview: ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of renowned VC firms. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law. Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Update your details, view your application and progress. Office of the Vice President and Provost 1 Job Alerts Keep informed about job opportunities at USD. Provost's Faculty Fellow in Research Development Apply now Posting #: 5287 Position Status: Faculty, Full-time regular Location: San Diego Position Type: Administrator, Faculty, Office of the Vice President and Provost Position Title & Department: Provost's Faculty Fellow in Research Development, Office of the Senior Vice President and Provost Posting # Posting # 5287 Department Description: The mission of Office of the Senior Vice President and Provost at USD is to provide academic leadership to its college and schools and promote excellence in all of the university's academic programs and initiatives, in order to educate ethical and compassionate leaders. University Description: The University of San Diego, a contemporary and engaged Roman Catholic institution , was founded by the Diocese of San Diego and the Society of the Sacred Heart in 1949. Governed by an independent board of trustees since 1972, USD remains committed to a liberal arts education grounded in the Catholic intellectual tradition and the pursuit of truth, goodness and beauty. Inspired by this centuries old tradition of Catholic higher education, the University welcomes people of all faith traditions and any, or no, religious background. The future success of USD relies on the contributions of those who seek to foster the development of engaged global citizens and an earnest confrontation of humanity's urgent challenges . Detailed Description: This recruitment is open to current University of San Diego tenured faculty only. The Provost's Faculty Fellow in Research Development will work closely with the Provost's team focusing on designing strategies and implementing initiatives to support and advance the university's research mission. This position will play an important role in strengthening USD's research culture, increasing faculty and student research productivity at both graduate and undergraduate levels, enhancing research infrastructure, funding resources and institutional visibility. Key responsibilities include: Strategic research development: support the implementation of the university's research vision and strategic goals; identify and promote interdisciplinary, community-based and global research collaborations; assist in developing and promoting institutional research initiatives aligned with USD's mission. Faculty engagement and support: organize and lead workshops, seminars, and grant development programs. Research infrastructure and tools: contribute to the development and promotion of research development tools; help assess and improve research support services. Recognition and visibility: collaborate with key stakeholders to highlight faculty research achievements through various communication channels; support initiatives that recognize and incentivize research excellence. Assessment and feedback: gather and analyze USD research community feedback; recommend improvements to research support structures and policies. The Provost's Faculty Fellow reports directly to and works under the general supervision of the Vice Provost for Research and Administration. The appointment will start on September 1, 2025. This position is renewable on an annual basis for up to three years. The Faculty Fellow will serve an estimated one month in the summer, with a teaching load of one 3-unit course within their respective discipline per Fall and Spring semester. The Faculty Fellow is expected to remain active in their ongoing faculty research and scholarship agenda. Job Requirements: USD tenured faculty member with a rank of associate or full professor A combination of at least six years of teaching and research at an accredited institution of higher education Demonstrated record of research excellence and external funding Experience with interdisciplinary or collaborative research preferred Successful administrative and professional development experience in a higher education institution Demonstrated ability to collaborate across units to improve efficiency and effectiveness of university procedures, programs, etc. Demonstrated ability to collaboratively lead and manage programs and/or a minimum of two years of academic leadership experience Demonstrated commitment to research excellence and innovation Strong communication, organizational and leadership skills Special Application Instructions: Click the "Apply Now" button to complete our online application. In addition, please upload a cover letter and CV to your application profile for the hiring managers' review. Review of applications will begin immediately with a priority deadline of July 18, 2025. The position will remain open until filled. If you have any technical questions or difficulties please contact the Employment Services Team ******************* Advertised: June 27, 2025 Pacific Daylight Time Applications close: Open until filled Notice of Availability: In compliance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (the Clery Act), the Annual Security and Fire Safety Report is available at ************************************************** . This report is published by October 1st of each year and includes current institutional policies and procedures concerning campus safety and security; fire safety and evacuation policies; sexual misconduct and relationship violence reporting and response stands and protocols; and crime and fire statistics for the three previous calendar years. To request a paper copy, please contact the Clery Act Compliance Manager via email at ****************** , by calling **************, or in-person in the Hughes Administration Center, room 150. #J-18808-Ljbffr

We are seeking a Microbiologist to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate. OID conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. Test specimens are collected from ongoing surveillance programs and from special investigations of febrile illnesses and pneumonia among military personnel or civilians (recruits, forces afloat, deployed forces, outbreaks of concern, and border populations). In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Results are provided to sponsors, the Armed Forces Health Surveillance Center, local investigators and collaborators, and, when applicable, county health units to guide proper responses that ultimately affect both the readiness of US forces and the safety of public health. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs. Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad. Responsibilities Pathogen Research & Characterization Develops laboratory workflows and optimizes assays to perform surveillance of target pathogens, particularly for wastewater. Utilizes molecular biology techniques, including concentration/extraction, quantitative PCR, and sequencing, to identify and characterize microbial genomes of pathogens. Works with a multi-functional team to ensure project deliverables are met. Oversees technology transfer of completed assays to the operational laboratory surveillance team, including documentation of standard operating procedures, validation/verification planning, and end-user training. Laboratory Management & Quality Control Ensures compliance with biosafety and biosecurity standards, especially when handling high-containment or potentially hazardous pathogens. Implements quality control measures to ensure the accuracy and reliability of experimental data and laboratory procedures. Collaboration & Research Support Collaborates with multidisciplinary research teams, including laboratory operations, immunologists, epidemiologists, and clinicians, to support infectious disease studies within the OID Directorate. Contributes to the design and implementation of research projects by providing microbiological expertise and ensuring proper experimental design and execution. Participates in field studies and operational research to monitor pathogen spread, assess environmental factors, and collect samples for microbiological analysis. Data Analysis & Reporting Analyzes and interprets microbiological data using advanced statistical and bioinformatics tools. Prepares scientific reports, manuscripts, and presentations for publication in peer-reviewed journals and presentations at scientific conferences. Contributes to grant writing and funding proposals by providing scientific insights, research plans, and data analysis frameworks. Qualifications PhD in Microbiology, Molecular Biology, or a related field. 1+ years of relevant experience in assay development and optimization, with a focus on infectious diseases. Proficiency in microbiological techniques, including microbial culture, pathogen isolation, molecular diagnostics (PCR, sequencing), and antimicrobial resistance testing. Strong understanding of assay development/optimization and data analysis. Experience with data analysis software, bioinformatics tools, and laboratory information management systems (LIMS). Strong problem-solving skills, attention to detail, and the ability to work independently and in collaboration with multidisciplinary teams. Excellent communication skills for presenting complex scientific data to diverse audiences. US Citizenship and the ability to obtain and maintain a T3/Secret Clearance. Please submit your resume online at *************** CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, political affiliation, marital status, military status, or any other characteristic protected by any applicable federal, state, or local law. CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability. Employment is contingent upon successful completion of a secret-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.

Job Title: Associate Scientist Duration: 2 Months Working Hours: Monday-Friday, 8:30am-5:30pm Focus: Downstream Process Development Role: The Associate Scientist/Sr Associate Scientist, Purification Process Development (Pivotal and Commercial) role will contribute to all aspects of purification development including process development and process characterization at internal or external facilities for client biologics entities during pivotal and commercial development phases. Specific Responsibilities: Contribute to experimental design. Plan and execute assigned purification process development laboratory studies. Support process scaleup and implementation in internal and external GMP facilities. Collect and analyze data from laboratory experiments in compliance with data integrity policy. Author experimental protocols and reports. Support process transfer to internal and contract manufacturing facilities to produce GMP and non GMP drug substances on time and with high success rate*** Provide technical support for manufacturing atypical event investigations. Ensure high-quality documentation in electronic laboratory notebooks, protocols and reports. Mentor junior team members on purification process development strategies, experimental design and execution as well as process transfer. Help to establish and maintain a state-of-the-art purification lab. Execute purification platform development and new technology/innovation evaluation and implementation to enable pivotal clinical trials. Participate in cross functional initiatives as needed. Adhere to department budget and all training, compliance and safety requirements. Education & Experience: M.S. with 3+ years or B.S. with 5+ years in a relevant scientific discipline (chemical engineering, biochemistry, bioengineering). Knowledge, Experience and Skills: Hands-on laboratory operations experience with purification process operations including centrifugation, normal flow filtration, chromatography operations, tangential flow filtration, and virus inactivation/removal is required. Experience with AKTA chromatography systems and UNICORN software is required Experience in pivotal stage purification process development, characterization, and implementation in GMP facilities. Antibody drug conjugate experience is a plus. Excellent communication, technical writing, and presentation skills and aptitude for creative problem solving. Experience writing CMC sections of commercial regulatory filings (BLA, MAA) and post approval change filings is a plus. Demonstrated ability to collaborate and influence cross-functionally. Experience in statistics, design-of-experiments, and data analysis (e.g. JMP, Spotfire). Working knowledge of lab automation, data management, data science, knowledge management and data protection is a plus Must Have's: Plan and execute assigned purification process development laboratory studies. Collect and analyze data from laboratory experiments in compliance with data integrity policy. Author experimental protocols and reports. Experience in pivotal stage purification process development, characterization, and implementation in GMP facilities Preferred Requirements: AKTA operation TFF Filtration/Viral Clearance Hamilton purification/High-throughput system operation

Performs study-related clinical procedures according to the study protocol and provides care under appropriate supervision for subjects enrolled in clinical trials. Performs duties in accordance with ProSciento's values, policies, and procedures. DUTIES AND RESPONSIBILITIES: * Understands the main objectives of each ongoing study and the study procedures for which he/she will be responsible. * Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, phlebotomy, and sample processing. * Demonstrates proficiency in documenting observations and study procedures correctly and legibly in the source document. * Understands and demonstrates proficiency in appropriately responding to medical emergencies onsite. * Performs study procedures as assigned. * Observes and records data related to patient safety and study procedures. * Ensures that all study data is recorded accurately and completely. * Assists nursing staff and Clinical Project Managers with study procedures and patient management as directed. * Assists in the transcription of study data from source documents to Case Report Forms (CRFs)/ (eCRFs). * Understands and complies with Good Clinical Practices (GCPs), particularly those regarding the protection of human subjects and integrity of clinical trial data. * Understands and complies with ProSciento Standard Operating Procedures (SOPs) and Work Instructions (WIs). * Participates as requested in ProSciento Continuous Quality Improvement (CQI) process. * Flexibility to work mornings, evenings, and/or overnight shifts as needed. * Attends and participates in all required training activities. * Participates as requested as a Clinical Operations Study Liaison. * Assists with Screening Receptionist duties and responsibilities as requested. * Assists with Recruitment duties and responsibilities as requested. JOB REQUIREMENTS / QUALIFICATIONS/EDUCATION: Qualifications: To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: High school diploma or general education degree (GED) as well as experience as a Medical Assistant, EMT, LVN, Phlebotomist, Foreign Medical Graduate (FMG), or Corpsman in a clinical or laboratory setting and/or equivalent combination of medical education, training, certifications, and/or experience. KNOWLEDGE, SKILLS, AND COMPETENCIES REQUIRED Skills, Knowledge, and Abilities: Able to perform basic clinical procedures correctly including vital signs, ECGs, and sample processing. Demonstrates initiative and problem-solving skills. Able to respect subject confidentiality and blinding procedures. Understands medical terminology and calculations. Demonstrates a strong attention to detail with superior organizational skills. Under general supervision, exercises judgment in accordance with well-defined policies, procedures, and techniques. Able to self-monitor progress and complete assigned tasks independently. Competencies: * Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment. * Peer Relationships: Can quickly find common ground and solve problems for the good of all; can represent his/her own interests and yet be fair to other groups; can solve problems with peers with a minimum of noise; is seen as a team player and is cooperative; easily gains trust and support of peers; encourages collaboration; can be candid with peers. * Process Management: Good at figuring out the processes necessary to get things done; knows how to organize people and activities; understands how to separate and combine tasks into efficient workflow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can't; can simplify complex processes; gets more out of fewer resources. * Action Oriented: Enjoys working hard; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others. * Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities; gets more done in less time than others; can attend a broader range of activities. Certificates and Licenses: * Basic Life Support (BLS) certification is required and may be provided by the company. GCP training is required and will be provided by the company. Language Skills: * Must be proficient in both verbal and written English. Able to communicate effectively with both employees and management. Ability to read and interpret documents such as safety rules, WIs, SOPs, medical terminology, and procedure manuals. Math Skills: * Able to add, subtract, multiply, and divide in all units of measure using whole numbers, fractions and decimals. Able to compute rate, ratio, and percent and to draw and interpret bar graphs. Reasoning Skills: * Ability to apply common sense understanding to carry out instructions provided in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Computer Skills: * To perform this job successfully an individual should have excellent computer skills with working knowledge in the current Microsoft Office Suite as well as Microsoft Windows operating systems. This position requires open availability for shift scheduling, including the ability to work any of the following shifts on an as-needed basis: 1st Shift (Day) 2nd Shift (Evening) 3rd Shift (Overnight) Candidates must also be available to work weekends and holidays, as coverage during these times may be required to meet operational needs.

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 As a Research Associate you will support the development of novel microfluidic platforms. You will be part of a multidisciplinary team solving complex problems, working on integration issues and investigating new research areas. Candidates that are engineering with a foundation in biology are better suited for this role vs. pure biologists. Hands-on testing, integration and optimization of microfluidic systems including fluidics, hardware, firmware, software, and chemistry/reagents Quickly fabricate and test prototyped microfluidic systems Conduct system level testing, assay testing, image analysis Translate benchtop assays to prototype microfluidic systems Use standard lab instrumentation: fluorescence plate readers, fluorescence microscopes, thermocyclers, bioanalyzers, DNA sequencers, syringe pumps Develop and implement experimental test plans Record and analyze complex data sets Develop creative solutions to troubleshoot issues Willingness to be hands-on Share and record experimental results for an audience with broad technical backgrounds at technical meetings Qualifications Skills: Microfluidics Experience with prototyping microfluidic systems: 3D printers, CO2 laser, laser ablation, profilometry Demonstrated ability to understand and successfully work across multiple disciplines including engineering, biology, and software is highly desired 1-2 years of experience in a clean room 1-2 years of experience in a lab environment with wet biology or chemistry experience 1-2 years of experience in product development is highly desired Experience in a BSL-2 lab is a plus Experience with sequencing, library prep and PCR is highly desired Organized and detail oriented Clear communicator and a team player Multidisciplinary approach to problem solving A desire to be part of face paced dynamic environment Education and Experience Undergraduate degree in Mechanical Engineering, Bioengineering, Chemical Engineering, Analytical Chemistry, or Physics Additional Information Vishnu Kumar Technical Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: *************** | Fax: ************

ABOUT SINGULAR GENOMICS Singular Genomics is inventing at the forefront of genomics, one of the world's fastest-growing industries. The commercially available G4 Sequencing Platform is a powerful, highly versatile benchtop genomic sequencer designed to produce fast and accurate results. In addition, the company is currently developing the G4X Spatial Sequencer, an upgrade to the G4, which will leverage Singular's proprietary sequencing technology, applying it as an in situ readout for transcriptomics, proteomics and fluorescent H&E in tissue, with spatial context. Singular Genomics' mission is to empower researchers and clinicians to advance science and medicine. We foster a culture of creativity and technical excellence, both catalysts for innovation. We celebrate diversity, emphasize collaboration and, as we rapidly mature, we are constantly looking at ways we can do better for our people. Our Headquarters are located on the Torrey Pines Mesa, in La Jolla, California at the center of the biotech hub. Our Manufacturing facility is in Sorrento Valley. Position Summary: As a Research Associate on the Histology team, you will be the foundation of platform development by maintaining and sectioning FFPE tissue blocks; support development of our proprietary tissue mounting system; use your background knowledge in histology and molecular diagnostics to identify controls, workflows, and enhancements to improve assay robustness and reliability; aid in expanding our assays to new tissue types, and provide guidance and expert advice to assay developers for interpreting results and expectations, and be the voice of histology when working with customers and collaborators. The ideal candidate will have a strong background in FFPE tissue sectioning and assessment using traditional histochemical staining such as H&E, familiarity in molecular assays on preserved tissue (e.g., IHC, IF, ISH/FISH) using a variety of microscopy readouts (brightfield, fluorescence etc.), and be comfortable following established complex assay workflows. You will be working with a multidisciplinary team of scientists in the fields of surface chemistry, engineering, biochemistry, and bioinformatics. This role is ideally suited to a candidate who is self-motivated and excited by a startup environment where opportunity to rise to frequent and diverse challenges is commonly encountered. Responsibilities: * Operate a microtome to produce consistent, high-quality FFPE tissue sections . * Support development teams by providing expert advice and guidance on tissue handling, experimental design, expectations, and interpretation of results. * QC FFPE tissues prior to using in assay development. * Actively contribute to optimizing in situ workflows. * Establish standards for onboarding and assessing performance of standard and new tissue types . * Collaboration and effective communication with team members in (surface) chemistry, biochemistry, systems integration, image analysis, and bioinformatics. * Maintain meticulous notes and databases of relevant reagents, experiments, equipment, and other processes. * Contribute to writing SOPs and other documentation. Qualifications: * B.S. in Biochemistry/biomedical sciences or related field plus 2-3+ years of histology experience. * 1-2 years of microtomy experience. * Hands on experience in precision microtomy with a focus on minimizing tissue loss of precious samples. * Understanding of healthy and diseased clinical samples is a plus. * Working knowledge of fluorescence microscopy is a plus. * Experience with molecular pathology assays (e.g., immunohistochemistry, in situ hybridization, immunofluorescence) and performance in different tissue types. Experience with multiplexed assays is strongly preferred. The estimated base salary range for this role based in the United States of America is: $68,640 - $92,800. Compensation decisions are dependent on several factors including, but not limited to, an individual's qualifications, location where the role is to be performed, internal equity, and alignment with market data. Should the level of the role change during the hiring process, the applicable salary range may be updated accordingly. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. Singular Genomics is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Singular Genomics is committed to working with and providing reasonable accommodations to job applicants with physical or mental disabilities. Applicants with a disability who require a reasonable accommodation for any part of the application or hiring process can provide their name and contact information to our Accommodations team at accommodationsrequest@singulargenomics.com. Your request will be responded to as soon as possible. Please note: Singular Genomics does not accept agency resumes and is not responsible for any fees related to unsolicited resumes. Please do not forward resumes to Singular Genomics employees.

In Vivo Research Associate II FLSA status: Non-Exempt Pay Rate: $28 - $32 /hr Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Medical Device department at the Research Associate II level. The Research Associate will play an important role by supporting in vivo studies to test medical devices. This position requires a broad knowledge of animal anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various indications. Responsibilities: * Experience in the administration of test substances by various basic methods (i.e., oral gavage, SQ, IV, dermal, etc.) * Manage and observe animals for general health and overall wellbeing. * Experience in the collection of biological specimens (i.e., blood from appropriate vessels from all species of laboratory animals at the site) * Able to perform study related activities in compliance with Good Laboratory Practice Regulations (GLPs), study protocols, and company policies and Standard Operating Procedures (SOPs) * Review documentation to ensure functions performed meet quality control requirements. * Handle, restrain, and provide care for all species of laboratory animals at the site. * Perform study preparation activities, including collection tube labeling and room setup. * Perform catheter placements in large animals. * Perform surgical procedure: intubation, anesthesia, pain recognition and analgesia. * Monitor animals under anesthesia and during post-operating monitoring and recovery. * Perform biopsies and skin excisions. * Perform necropsies and tissue collection. * Interface with different teams, including study director, principal investigator, QC/QA, and Account Managers/Sales. * Maintain accurate records in various internal databases. * Support internal research projects to optimize service offerings. Perform aseptic techniques. * Perform other duties as directed by management. What We're Looking For: * We're seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments. * Associates degree (preferred) in veterinary technology with 3 years relevant experience. * BS with at least 2 years relevant experience. * Education level requirements could be amended based on relevant years of experience. * Certification as a registered veterinarian technician (RVT) is a plus. * Background in lab animal (in vivo) research is a must. * Working knowledge of preclinical techniques and modalities will be a plus. * Position requires good communication skills and attention to detail. * Strong work ethic, self-motivation, and ability to adapt to a dynamic team environment. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package: * Insurance including Medical, Dental & Vision with significant employer contributions * Employer-funded Health Reimbursement Account * Healthcare & Dependent Care Flexible Spending Accounts * 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance * 401k plan with generous employer match * Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #LI-MC1

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: Requirements/ have to haves not listed elsewhere: Bachelor's Degree Request preferences/ nice to haves: Molecular biology experience, Sequencing, Plasmid prep Primary Position Responsibilities (major or daily tasks): DNA Sequencing Sequencing/ DNA Cloning/Vector prep Key Objectives/Deliverables: • Assist in performing DNA Sequencing reactions • Operation of liquid handling automation • Work collaboratively with other groups to achieve objectives and timelines. Basic Requirements • Basic Molecular Biology knowledge and experience such as PCR, plasmid purification, cloning, agarose and polyacrylamide gel electrophoresis and restriction digests. • Ability to work in a team environment. • Attention to detail. Additional Preferences • DNA Sequencing • Biomek Robot experience • Capillary Electrophoresis Education Requirements • Bachelor's Degree or equivalent work experience. Qualifications Requirements/ have to haves not listed elsewhere: Bachelor's Degree Request preferences/ nice to haves: Molecular biology experience, Sequencing, Plasmid prep Primary Position Responsibilities (major or daily tasks): DNA Sequencing Additional Information All your information will be kept confidential according to EEO guidelines.

Research Biologist needs 1 or more years of research experience in an academic institute, biotechnology or pharmaceutical industry Research Biologist requires: Bachelors degree in biology, biochemistry, molecular biology or similar discipline with 1 or more years of research experience in an academic institute, biotechnology or pharmaceutical industry Experience in running biochemical and immunological assays. Highly motivated and agile biochemist Research Biologist duties: Perform experiments to characterize protein-protein interactions using PAGE, Western Blot, ELISA & SPR technologies Perform basic tasks to support tissue culture and maintenance of immune competent cell lines Perform basic cell-based assays with immunology research-related technologies (e.g. human whole blood, primary human leukocyte isolation, cellular activation and differentiation, FACS, cytokine assay, etc.) Work with a cross-disciplinary team for data analysis Independently execute experiments, analyze, interpret and present experimental data

ABOUT US: Scripps Research is a nonprofit biomedical institute ranked as one of the most influential in the world for its impact on innovation. We are celebrating our 100-year legacy. This significant milestone marks a century of seminal discoveries in immunology, infectious diseases (such as COVID-19, flu, HIV), neuroscience, heart disease, cancer, and more. Located in La Jolla, California, the institute houses six research departments, multiple Nobel laureates, a top-ranked graduate school and a leading postdoctoral training program. We work hand-in-hand with researchers of the Scripps Research Translational Institute and Calibr to merge foundational studies in biology, chemistry and computer science with translational science to produce pioneering drugs and advances in digital and precision medicine. Together, we cultivate new scientific leaders and expand the frontiers of knowledge to deliver medical breakthroughs impacting human health around the globe. If you have a passion for making a difference, this could be your opportunity to join our transformative team. Celebrating a Century: ************************ POSITION TITLE: Research Technician POSITION SUMMARY: The Department of Neuroscience at Scripps Research has open positions in the new lab of Dr. Chen Ran. We are interested in understanding, on the cellular, circuit, and systems levels, the neural basis of interoception, i.e., how the brain receives signals from the visceral organs within the body to generate our internal senses. We seek to unravel how the nervous system detects mechanical, chemical, and thermal stimuli from the periphery to synthesize our internal sensations, including satiety, hunger, nausea, hypoxia, and visceral pain. We use state-of-the-art in vivo functional imaging, electrophysiological recordings, mouse genetics, neuronal activity manipulation, animal behavior, and computational approaches (Ran et al., Nature, 2022). Through our research, we will reveal fundamental principles governing how the brain encodes and processes information. This will, in turn, pave the way for the development of novel therapeutics for various diseases, including hypertension, obesity, diabetes, indigestion, eating disorders, pulmonary diseases, nausea, visceral pain, and infection-induced sickness behaviors. Find out more from our group website: ************************* We encourage individuals who are seeking to gain intensive 2-3 year research experience prior to applying to PhD programs or medical schools. This position involves comprehensive training in science and individualized mentorship. Previous technicians and undergraduate trainees of Dr. Ran were accepted into top-tier programs, including UCSF, Stanford, UCSD, Columbia, and others. This position will provide a strong research foundation to enhance application competitiveness. Additionally, technicians who are eager to pursue PhD study can be recruited through the graduate programs at Scripps or UCSD. RESPONSIBLITIES AND DUTIES: The Research Technician will work with the Principal Investigator and members of the lab as needed to advance current projects. This individual will be listed as a co-author on publications for the projects he/she contributes to and gain valuable bench-side and analytical experience in a fast-paced research environment. * Additional responsibilities include: * Ensure laboratory personnel are maintaining a clean, organized workspace. * Maintain laboratory inventory and responsible for ordering reagents and other supplies. * Place maintenance requests for laboratory apparatus and facility. * Participate in weekly lab meetings by reporting data and presenting during journal clubs. * Genotype and maintain mouse colonies. * Provide support with general laboratory maintenance and compliance with health and safety policies, and help to train, supervise, and mentor junior staff as needed. REQUIREMENTS: * Recently (i.e., no earlier than 2020) obtained a Bachelor's (or Master's) degree in a relevant scientific discipline. * At least 2 years of lab experience. * Energetic, bright, and highly motivated candidates with backgrounds in biology, neuroscience, biochemistry, molecular biology, genetics, bioengineering, physiology, or psychology are especially encouraged to apply. * International candidates should be eligible for F-1 OPT to be authorized to work at Scripps. * The ideal candidate can engage in extensive animal work, including surgeries and dissections. PHYSICAL REQUIREMENTS: * This position works in a laboratory and a vivarium environment. * Details of established/essential functions for this position will be addressed/discussed during the interview process. COMPENSATION: The expected hiring range for this position is $18.67 to $24 per hour, commensurate with experience. Consideration will be given to experience that exceeds the listed requirements. COMPREHENSIVE BENEFITS INCLUDE: * Employer Contributed Retirement Plan - Depending on eligibility, employees receive an employer contributed retirement plan (no employee contribution required) and the option to contribute to a 403(b) (which is similar to a 401(k) using your own pre or post-tax dollars) * Full Suite of Health and Welfare plans including three medical plan options (including an HSA available option), dental, vision, life insurance, disability, EAP and more * Access to Flexible Spending Accounts (Medical/Dependent Care) * Competitive vacation and sick leave policies * Free, on-site parking The above statements describe the level of work performed and expected in general terms. The statements are not intended to list all the responsibilities, duties and/or skills required of employees so classified, and the content herein is subject to change due to the business needs of Scripps Research, with or without notice. Furthermore, nothing in this job description shall be interpreted to be in conflict with or to eliminate or modify in any way the employment-at-will status of Scripps Research staff. EEO Statement: The Scripps Research Institute is an Equal Opportunity Employer. We promote diversity of thought, culture and background in the fields of science. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic or status.

Performs study-related clinical procedures according to the study protocol and provides care under appropriate supervision for subjects enrolled in clinical trials. Performs duties in accordance with ProSciento's values, policies, and procedures. DUTIES AND RESPONSIBILITIES: Understands the main objectives of each ongoing study and the study procedures for which he/she will be responsible. Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, phlebotomy, and sample processing. Demonstrates proficiency in documenting observations and study procedures correctly and legibly in the source document. Understands and demonstrates proficiency in appropriately responding to medical emergencies onsite. Performs study procedures as assigned. Observes and records data related to patient safety and study procedures. Ensures that all study data is recorded accurately and completely. Assists nursing staff and Clinical Project Managers with study procedures and patient management as directed. Assists in the transcription of study data from source documents to Case Report Forms (CRFs)/ (eCRFs). Understands and complies with Good Clinical Practices (GCPs), particularly those regarding the protection of human subjects and integrity of clinical trial data. Understands and complies with ProSciento Standard Operating Procedures (SOPs) and Work Instructions (WIs). Participates as requested in ProSciento Continuous Quality Improvement (CQI) process. Flexibility to work mornings, evenings, and/or overnight shifts as needed. Attends and participates in all required training activities. Participates as requested as a Clinical Operations Study Liaison. Assists with Screening Receptionist duties and responsibilities as requested. Assists with Recruitment duties and responsibilities as requested. JOB REQUIREMENTS / QUALIFICATIONS/EDUCATION: Qualifications: To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: High school diploma or general education degree (GED) as well as experience as a Medical Assistant, EMT, LVN, Phlebotomist, Foreign Medical Graduate (FMG), or Corpsman in a clinical or laboratory setting and/or equivalent combination of medical education, training, certifications, and/or experience. KNOWLEDGE, SKILLS, AND COMPETENCIES REQUIRED Skills, Knowledge, and Abilities: Able to perform basic clinical procedures correctly including vital signs, ECGs, and sample processing. Demonstrates initiative and problem-solving skills. Able to respect subject confidentiality and blinding procedures. Understands medical terminology and calculations. Demonstrates a strong attention to detail with superior organizational skills. Under general supervision, exercises judgment in accordance with well-defined policies, procedures, and techniques. Able to self-monitor progress and complete assigned tasks independently. Competencies: Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment. Peer Relationships: Can quickly find common ground and solve problems for the good of all; can represent his/her own interests and yet be fair to other groups; can solve problems with peers with a minimum of noise; is seen as a team player and is cooperative; easily gains trust and support of peers; encourages collaboration; can be candid with peers. Process Management: Good at figuring out the processes necessary to get things done; knows how to organize people and activities; understands how to separate and combine tasks into efficient workflow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can't; can simplify complex processes; gets more out of fewer resources. Action Oriented: Enjoys working hard; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others. Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities; gets more done in less time than others; can attend a broader range of activities. Certificates and Licenses: Basic Life Support (BLS) certification is required and may be provided by the company. GCP training is required and will be provided by the company. Language Skills: Must be proficient in both verbal and written English. Able to communicate effectively with both employees and management. Ability to read and interpret documents such as safety rules, WIs, SOPs, medical terminology, and procedure manuals. Math Skills: Able to add, subtract, multiply, and divide in all units of measure using whole numbers, fractions and decimals. Able to compute rate, ratio, and percent and to draw and interpret bar graphs. Reasoning Skills: Ability to apply common sense understanding to carry out instructions provided in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Computer Skills: To perform this job successfully an individual should have excellent computer skills with working knowledge in the current Microsoft Office Suite as well as Microsoft Windows operating systems. This position requires open availability for shift scheduling, including the ability to work any of the following shifts on an as-needed basis: 1st Shift (Day) 2nd Shift (Evening) 3rd Shift (Overnight) Candidates must also be available to work weekends and holidays, as coverage during these times may be required to meet operational needs.

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 As a Research Associate you will support the development of novel microfluidic platforms. You will be part of a multidisciplinary team solving complex problems, working on integration issues and investigating new research areas. Candidates that are engineering with a foundation in biology are better suited for this role vs. pure biologists. Hands-on testing, integration and optimization of microfluidic systems including fluidics, hardware, firmware, software, and chemistry/reagents Quickly fabricate and test prototyped microfluidic systems Conduct system level testing, assay testing, image analysis Translate benchtop assays to prototype microfluidic systems Use standard lab instrumentation: fluorescence plate readers, fluorescence microscopes, thermocyclers, bioanalyzers, DNA sequencers, syringe pumps Develop and implement experimental test plans Record and analyze complex data sets Develop creative solutions to troubleshoot issues Willingness to be hands-on Share and record experimental results for an audience with broad technical backgrounds at technical meetings Qualifications Skills: Microfluidics Experience with prototyping microfluidic systems: 3D printers, CO2 laser, laser ablation, profilometry Demonstrated ability to understand and successfully work across multiple disciplines including engineering, biology, and software is highly desired 1-2 years of experience in a clean room 1-2 years of experience in a lab environment with wet biology or chemistry experience 1-2 years of experience in product development is highly desired Experience in a BSL-2 lab is a plus Experience with sequencing, library prep and PCR is highly desired Organized and detail oriented Clear communicator and a team player Multidisciplinary approach to problem solving A desire to be part of face paced dynamic environment Education and Experience Undergraduate degree in Mechanical Engineering, Bioengineering, Chemical Engineering, Analytical Chemistry, or Physics Additional Information Vishnu Kumar Technical Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: *************** | Fax: ************

Job Description In Vivo Research Associate II FLSA status: Non-Exempt Pay Rate: $28 - $32 /hr Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Medical Device department at the Research Associate II level. The Research Associate will play an important role by supporting in vivo studies to test medical devices. This position requires a broad knowledge of animal anatomy, physiology, and biochemistry to help develop and support in vivo models to screen therapeutics and devices being developed for various indications. Responsibilities: Experience in the administration of test substances by various basic methods (i.e., oral gavage, SQ, IV, dermal, etc.) Manage and observe animals for general health and overall wellbeing. Experience in the collection of biological specimens (i.e., blood from appropriate vessels from all species of laboratory animals at the site) Able to perform study related activities in compliance with Good Laboratory Practice Regulations (GLPs), study protocols, and company policies and Standard Operating Procedures (SOPs) Review documentation to ensure functions performed meet quality control requirements. Handle, restrain, and provide care for all species of laboratory animals at the site. Perform study preparation activities, including collection tube labeling and room setup. Perform catheter placements in large animals. Perform surgical procedure: intubation, anesthesia, pain recognition and analgesia. Monitor animals under anesthesia and during post-operating monitoring and recovery. Perform biopsies and skin excisions. Perform necropsies and tissue collection. Interface with different teams, including study director, principal investigator, QC/QA, and Account Managers/Sales. Maintain accurate records in various internal databases. Support internal research projects to optimize service offerings. Perform aseptic techniques. Perform other duties as directed by management. What We're Looking For: We're seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments. Associates degree (preferred) in veterinary technology with 3 years relevant experience. BS with at least 2 years relevant experience. Education level requirements could be amended based on relevant years of experience. Certification as a registered veterinarian technician (RVT) is a plus. Background in lab animal (in vivo) research is a must. Working knowledge of preclinical techniques and modalities will be a plus. Position requires good communication skills and attention to detail. Strong work ethic, self-motivation, and ability to adapt to a dynamic team environment. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators. Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package: Insurance including Medical, Dental & Vision with significant employer contributions Employer-funded Health Reimbursement Account Healthcare & Dependent Care Flexible Spending Accounts 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance 401k plan with generous employer match Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #LI-MC1

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Duration: 18+ months (Possible Of Extension) Location: San Diego, CA Job Details: Conduct experiments to identify and validate drug targets. Support assay design, optimization, validation, and data analyses. Design and execute molecular and cell biology experiments. Troubleshoot and analyze complex data in support of drug discovery projects. Presentation of results and conclusions both orally and written. Candidate will need to have experience in molecular biology, experimental design and biological technical skills. This candidate will be performing in a high paced environment most items will be trained on site, looking for the strong candidate that has a great behavior, excellent attitude, high learning agility, good team player with above par communication skills. It would be nice if they have experience in Vecteector and NTI sequencing software but it is not required. This will be a great experience for someone who wants to learn new things. Additional Information All your information will be kept confidential according to EEO guidelines.

Research Biologist needs 2-3 years experience Research Biologist requires: Degree in biology Laboratory equipment and procedures. MS Office Lab techniques Research Biochemistry Cell biology Experience in running biochemical and immunological assays. Research Biologist duties: Ø Conduct experiments to identify and validate drug targets. Ø Support assay design, optimization, validation, and data analyses. Ø Design and execute molecular and cell biology experiments. Ø Troubleshoot and analyze complex data in support of drug discovery projects. Ø Presentation of results and conclusions both orally and written.

ABOUT US: Scripps Research is a nonprofit biomedical institute ranked as one of the most influential in the world for its impact on innovation. We are celebrating our 100-year legacy. This significant milestone marks a century of seminal discoveries in immunology, infectious diseases (such as COVID-19, flu, HIV), neuroscience, heart disease, cancer, and more. Located in La Jolla, California, the institute houses six research departments, multiple Nobel laureates, a top-ranked graduate school and a leading postdoctoral training program. We work hand-in-hand with researchers of the Scripps Research Translational Institute and Calibr to merge foundational studies in biology, chemistry and computer science with translational science to produce pioneering drugs and advances in digital and precision medicine. Together, we cultivate new scientific leaders and expand the frontiers of knowledge to deliver medical breakthroughs impacting human health around the globe. If you have a passion for making a difference, this could be your opportunity to join our transformative team. Celebrating a Century: ************************ POSITION TITLE: Research Technician RESPONSIBILITIES AND DUTIES: Record data providing basic analyses and interpretations Conduct experiments, analyze resulting data and troubleshoot experimental issues while delivering comprehensive oral and written reports Generate constructs, reagents and cell lines genotype Maintain mouse colonies Provide support with general laboratory maintenance and compliance with health and safety policies Train, supervise and mentor junior staff as needed Other related duties, tasks and responsibilities as required or assigned REQUIREMENTS: Requires a bachelor's degree in a relevant scientific discipline and up to one (1) year of related experience. Three (3) to six (6) years of related laboratory experience may be considered in lieu of a degree. COMPENSATION: The expected hiring range for this position is $18.67 to $24 per hour, commensurate with experience. Consideration will be given to experience that exceeds the listed requirements. COMPREHENSIVE BENEFITS INCLUDE: Employer Contributed Retirement Plan - Depending on eligibility, employees receive an employer contributed retirement plan (no employee contribution required) and the option to contribute to a 403(b) (which is similar to a 401(k) using your own pre or post-tax dollars) Full Suite of Health and Welfare plans including three medical plan options (including an HSA available option), dental, vision, life insurance, disability, EAP and more Access to Flexible Spending Accounts (Medical/Dependent Care) Competitive vacation and sick leave policies Free, on-site parking The above statements describe the level of work performed and expected in general terms. The statements are not intended to list all the responsibilities, duties and/or skills required of employees so classified, and the content herein is subject to change due to the business needs of Scripps Research, with or without notice. Furthermore, nothing in this job description shall be interpreted to be in conflict with or to eliminate or modify in any way the employment-at-will status of Scripps Research staff. EEO Statement: The Scripps Research Institute is an Equal Opportunity Employer. We promote diversity of thought, culture and background in the fields of science. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic or status.

Job Description Performs study-related clinical procedures according to the study protocol and provides care under appropriate supervision for subjects enrolled in clinical trials. Performs duties in accordance with ProSciento’s values, policies, and procedures. DUTIES AND RESPONSIBILITIES: Understands the main objectives of each ongoing study and the study procedures for which he/she will be responsible. Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, phlebotomy, and sample processing. Demonstrates proficiency in documenting observations and study procedures correctly and legibly in the source document. Understands and demonstrates proficiency in appropriately responding to medical emergencies onsite. Performs study procedures as assigned. Observes and records data related to patient safety and study procedures. Ensures that all study data is recorded accurately and completely. Assists nursing staff and Clinical Project Managers with study procedures and patient management as directed. Assists in the transcription of study data from source documents to Case Report Forms (CRFs)/ (eCRFs). Understands and complies with Good Clinical Practices (GCPs), particularly those regarding the protection of human subjects and integrity of clinical trial data. Understands and complies with ProSciento Standard Operating Procedures (SOPs) and Work Instructions (WIs). Participates as requested in ProSciento Continuous Quality Improvement (CQI) process. Flexibility to work mornings, evenings, and/or overnight shifts as needed. Attends and participates in all required training activities. Participates as requested as a Clinical Operations Study Liaison. Assists with Screening Receptionist duties and responsibilities as requested. Assists with Recruitment duties and responsibilities as requested. JOB REQUIREMENTS / QUALIFICATIONS/EDUCATION: Qualifications: To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: High school diploma or general education degree (GED) as well as experience as a Medical Assistant, EMT, LVN, Phlebotomist, Foreign Medical Graduate (FMG), or Corpsman in a clinical or laboratory setting and/or equivalent combination of medical education, training, certifications, and/or experience. KNOWLEDGE, SKILLS, AND COMPETENCIES REQUIRED Skills, Knowledge, and Abilities: Able to perform basic clinical procedures correctly including vital signs, ECGs, and sample processing. Demonstrates initiative and problem-solving skills. Able to respect subject confidentiality and blinding procedures. Understands medical terminology and calculations. Demonstrates a strong attention to detail with superior organizational skills. Under general supervision, exercises judgment in accordance with well-defined policies, procedures, and techniques. Able to self-monitor progress and complete assigned tasks independently. Competencies: Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment. Peer Relationships: Can quickly find common ground and solve problems for the good of all; can represent his/her own interests and yet be fair to other groups; can solve problems with peers with a minimum of noise; is seen as a team player and is cooperative; easily gains trust and support of peers; encourages collaboration; can be candid with peers. Process Management: Good at figuring out the processes necessary to get things done; knows how to organize people and activities; understands how to separate and combine tasks into efficient workflow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can’t; can simplify complex processes; gets more out of fewer resources. Action Oriented: Enjoys working hard; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others. Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities; gets more done in less time than others; can attend a broader range of activities. Certificates and Licenses: Basic Life Support (BLS) certification is required and may be provided by the company. GCP training is required and will be provided by the company. Language Skills: Must be proficient in both verbal and written English. Able to communicate effectively with both employees and management. Ability to read and interpret documents such as safety rules, WIs, SOPs, medical terminology, and procedure manuals. Math Skills: Able to add, subtract, multiply, and divide in all units of measure using whole numbers, fractions and decimals. Able to compute rate, ratio, and percent and to draw and interpret bar graphs. Reasoning Skills: Ability to apply common sense understanding to carry out instructions provided in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Computer Skills: To perform this job successfully an individual should have excellent computer skills with working knowledge in the current Microsoft Office Suite as well as Microsoft Windows operating systems. This position requires open availability for shift scheduling, including the ability to work any of the following shifts on an as-needed basis: 1st Shift (Day) 2nd Shift (Evening) 3rd Shift (Overnight) Candidates must also be available to work weekends and holidays, as coverage during these times may be required to meet operational needs.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Its a simple route driver job and company will be providing the car. Job Description: Requirements/ have to haves not listed elsewhere: Bachelor's Degree Request preferences/ nice to haves: Molecular biology experience, Sequencing, Plasmid prep Primary Position Responsibilities (major or daily tasks): DNA Sequencing Sequencing/ DNA Cloning/Vector prep Key Objectives/Deliverables: • Assist in performing DNA Sequencing reactions • Operation of liquid handling automation • Work collaboratively with other groups to achieve objectives and timelines. Basic Requirements • Basic Molecular Biology knowledge and experience such as PCR, plasmid purification, cloning, agarose and polyacrylamide gel electrophoresis and restriction digests. • Ability to work in a team environment. • Attention to detail. Additional Preferences • DNA Sequencing • Biomek Robot experience • Capillary Electrophoresis Education Requirements • Bachelor's Degree or equivalent work experience. Qualifications Requirements/ have to haves not listed elsewhere: Bachelor's Degree Request preferences/ nice to haves: Molecular biology experience, Sequencing, Plasmid prep Primary Position Responsibilities (major or daily tasks): DNA Sequencing Additional Information All your information will be kept confidential according to EEO guidelines.