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Clinical Outcome Assessment (COA) Lead

Sanofi
Morristown, NJ Full Time
POSTED ON 4/25/2026
AVAILABLE BEFORE 5/24/2026
Job title: Clinical Outcome Assessment (COA) Lead

  • Location: Morristown, NJ

About The Job

The remit of the Clinical Outcome Assessment (COA) team at Sanofi is to incorporate the patients’ perspective (and other subjective perspectives) into clinical research through the utilization of Clinical Outcome Assessments (COAs) and other methods.

Example research activities for the COA team include the development of a disease conceptual model; the selection of COA instruments to measure specific concepts of interest; the psychometric assessment of the measurement properties of a COA instruments; the development and validation of new COA instruments; the development of briefing books or dossiers for regulatory consideration of COAs.

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 Job Responsibilities

The COA Lead is accountable for the definition of COA endpoint strategies and responsible for the conduct of related activities in relation to specific programs, assets or indications. The scope evolves as the COA Lead gains experience in role and demonstrates ability to take more in quantity (TA portfolio), impact (primary and key secondary endpoints) and exposure (strategic assets or indications).

Main Responsibilities Also Include

  • Contribute to the Target Value Proposition with respect to patient-centric outcomes value messaging.
  • Contribute to a successful strategy for innovative product by an optimized COA endpoint strategy aligned with Sanofi’s Best In Class / First In Class approach.
  • Generate a comprehensive understanding of a disease and treatment paradigm through primary and secondary research.
  • Advise on the use and/or development of Fit-for-Purpose COA instruments in clinical research projects; including gap analyses, implementation, statistical analyses, psychometric validation and dissemination.
  • Manage the qualitative and quantitative research projects to close the validation gap(s) on the selected COA instruments (including vendor management).
  • Prepare the scientific documents (reports, regulatory documents, publications,...) for internal and external communication.
  • Leads specific internal organizational initiatives, within COA and PID-HVT (eg. RACI, templates, guidance).
  • Advocate for the role of quantitative and qualitative COA across Sanofi, participate in creating and delivering education on COAs for internal business partners.
  • Mentor more junior COA scientists, share specific knowledge and expertise with the COA team; provide direction and delegate specific tasks to associate COA scientist.
  • Implement new methodologies and promote innovative approaches.
  • Define or update overarching approach and framework to COA endpoints strategies in strategic area (eg Oncology, I&I, rare diseases).

About You

Main Qualifications:

  • Bachelor's degree is required; Master's degree is preferred (not mandatory), in fields of study such as Psychology, Anthropology, Sociology, Public Health, Epidemiology, Psychometrics, Clinical Research, Physiotherapy, Pharmacy, Medicine, Biostatistics, and other related disciplines.
  • Minimum 3 years of relevant experience in COA in Pharma/CRO/Consultancy: ideally proven track record from scientific publications in core COA disciplines such as COA data analyses and/or creation or validation of new COAs and/or COA endpoint strategy implementation.
  • Knowledge of the drug development process and the regulatory (FDA, EMA, local agencies) and payer (EUnetHTA, NICE, HAS, G-BA, other local agencies) environment.

Preferred Qualification

  • Strong analytical and synthesis skills of qualitative and quantitative data.
  • Accountability and hands-on mindset, autonomy and sense of initiative.
  • Good interpersonal and communication skills, both written and oral.
  • Ability to manage multiple priorities and projects, and balance workload and timelines.

Why Choose Us

  • 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 millions of people globally by making drug development quicker and more effective.
  • Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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$91,259 to $113,062
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