Senior Scientist I - Biomarkers and Clinical Bioanalyses
SanofiAbout the role
Job Title: Senior Scientist I - Biomarkers and Clinical Bioanalyses
Location: Cambridge, MA
About the Job:
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
We are seeking a Senior Scientist to join the Functional Biomarker Team within Laboratory Sciences (Lab Sci), a global department in the Translational Medicine Unit (TMU) at Sanofi.
In this role, the scientist will lead method development and validation of complex assays, implement testing strategies, and execute clinical projects within controlled timelines. The role also includes preparing reports suitable for regulatory submissions to support clinical development.
The ideal candidate will have hands-on experience with Spectral flow cytometry instrumentation and troubleshooting, high-parameter panel development, and the analytical interpretation of results. This position operates in a matrixed global team environment and requires strong collaboration skills.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
Independently develop, validate, and implement complex bioanalytical assays to support testing in nonclinical and clinical studies, with a focus on immunophenotyping panels and/or receptor occupancy/density methods by flow cytometry
Serve as responsible scientist for regulated studies, providing scientific oversight, data interpretation, and ensuring compliance with internal best practices and regulatory guidance
Oversee and mentor junior analysts in method validation and sample testing; offer scientific rationale for assay development and troubleshooting
Author SOPs, study plans, reports, and abstracts, producing high-quality documents requiring minimal editing
Present scientific data to internal and external stakeholders
Lead regulatory and safety compliance efforts in the laboratory; champion process improvement initiatives to drive operational excellence
Manage multiple project commitments under tight timelines
Serve as bioanalytical lead on global project teams
Collaborate with global teams to design and implement testing strategies for ongoing and future clinical programs
Ensure timely readiness of validated methods to meet critical deliverables
Work with outsourcing operations and CROs to transfer and manage external testing; act as subject matter expert in reviewing and troubleshooting CRO development and validation studies
Contribute to the TMU's mission in conducting reverse translational studies
About You:
Basic Qualifications:
Ph.D. in a life sciences field with 3+ years of bioanalytical industry experience in a regulated environment, OR Master’s degree with 5+ years of experience, OR Bachelor’s degree with 10+ years of experience
A degree in Immunology, Biochemistry, or Biology is preferred
Experience working with CROs and external testing partners, with the ability to lead technology transfer and troubleshoot assay validation
Minimum 5+ years of experience with key analytical software (e.g., SoftMax, FlowJo, FCS Express), and proficiency in statistical software such as Excel, JMP, GraphPad Prism
Strong written and oral communication skills, with demonstrated ability to collaborate effectively in a team
Proven problem-solving skills and scientific leadership in assay troubleshooting and optimization
Solid understanding of bioanalytical method development, industry best practices, and regulatory expectations (FDA/EMA) for method validation
Experience in a GCLP-regulated environment supporting nonclinical and clinical development
Experience supervising and guiding junior scientists in assay development and execution will be a plus
Preferred Qualifications:
Experience with Watson LIMS or similar laboratory information management systems
Familiarity with electronic laboratory notebooks e.g. Benchling
Understanding of biological sample collection techniques and suitability for different assay types
Experience wi
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