Research Associate, Clinical Research, Medical Science
Listed on 2026-03-12
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Job title: Research Associate
- Location:
Swiftwater, PA
The Global Clinical Immunology (GCI) organization, part of Late Stage Global Immunology within Vaccines R&D, specializes in developing, validating, and deploying regulated bioanalytical assays to assess immune responses to vaccines throughout their lifecycle. Our mission is to provide specialized immunology expertise and generate robust clinical datasets that inform decision-making for both clinical development and post‑licensure activities. Our GCLP‑compliant bioanalytical laboratories are based in Swiftwater, PA.
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI‑powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.
About Sanofi:We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:Laboratory testing and support activities as assigned including:
- Routine and non‑routine testing
- Maintenance of any associated testing documentation
- Sample/reagent handling
Laboratory support activities including, but not limited to:
- Responsible for and/or performs lab and/or facility housekeeping, waste, and general maintenance
- Ensures that security and safety procedures are observed and followed.
- Monitors, maintains laboratory inventory; responsible for reagent/material orders, receipt and delivery of laboratory reagent/material and equipment.
- Training coworkers, including interns, on laboratory methods, procedures and techniques; assist with the generation of training modules as needed.
- Scientific data review and approval
- Document generation associated with project/objectives. This may include, but is not limited to, protocols, reports, operating procedures/instructions, regulatory correspondence, or presentations.
Regulatory/Quality Management:
- Support departmental quality by ensuring adequate support for documentation, investigation, and closure of quality items including change controls, deviations, and CAPAs.
- Ensures adherence to all applicable quality, corporate, safety, and regulatory requirements.
Other:
- As assigned and under the direction of management, independently conducts more complex research activities in support of short‑and‑long‑term laboratory operational requirements.
- Any other related duties required by the research projects or management of the research laboratory or analytical facility.
Education:
Bachelor's degree in Biology, Biological Sciences, Microbiology, Biochemistry, Molecular Biology, or a related scientific field.
Experience:
1–2 years of professional experience in a laboratory analyst or research associate role.
Industry Background:
Experience in the pharmaceutical or biopharmaceutical industry is strongly preferred — candidates with 1–2 years specifically in pharma/biopharma will be prioritized.
Hands‑on experience in Molecular Biology, with a strong focus on Next Generation Sequencing (NGS).
Proficiency in NGS data analysis and interpretation of sequencing results.
Practical skills in nucleic acid extraction, PCR, and digital PCR (dPCR).
- Bring the miracles of science to life alongside a supportive, future‑focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs and at least 14 weeks’ gender‑neutral parental leave.
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real‑world needs.
- Help improve the lives of…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).