Senior Principal Scientist I – Functional Biomarkers Full-time

Senior Principal Scientist I – Functional Biomarkers

Location: Cambridge, MA

Functional group leader in the US Laboratory Sciences group, a global department within the Translational Medicine Unit of Sanofi. The individual in this position will lead a group of scientists and analysts to develop, validate and implement complex immunophenotyping panels and functional biomarker assays in a regulated environment. The successful candidate should have an extensive background in flow cytometry instrumentation and troubleshooting, high-parameter panel development, and cell sorting along with expertise in assay design, method validation, and analytical interpretation of results along with proven people management skills.

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.

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:

• Lead and manage local teams to develop, validate, and implement complex cell staining panels upwards of 30+ colors according to, or exceeding the highest scientific and applicable regulatory (GLP, GCLP) standards.
• Oversee method development and/or transfer and implementation of complex immunophenotyping panels at dedicated CROs.
• Serve as a flow cytometry subject matter expert; provide scientific oversight and data interpretation and ensure data generated internally or with CROs meets compliance requirements according to internal best practices and regulatory guidance.
• Serve as bioanalytical lead on global project teams:
• Work with global teams to develop and operationalize testing strategies to support new and ongoing clinical programs.
• Ensure that all methods are in place to meet critical deliverables.
• Lead team to prepare high quality standard operating procedures, study plans and reports.
• Lead global Sanofi efforts to develop best practices and guidance documents for regulated bioanalysis.
• Contribute to implementation of best practices industry-wide through participation in external scientific organizations
• Take a leadership role in ensuring regulatory and safety compliance in the laboratory; promote operational excellence by leading process improvement efforts.
• Prioritize multiple project commitments under the confines of challenging timelines. Plan proactively, anticipating challenges and future goals. Make decisions readily understanding the impact on Sanofi success and demonstrate agility relating to change.
• Lead efforts to implement AI tools to streamline method development and data analysis workflows.

About You

Basic Qualifications:

• Ph.D. degree in the field of immunology, biochemistry, biology, or other life-science field with 7+ years of post-graduate industry or research experience, or Master's degree in a similar field with 10+ years of industry or research experience.
• Expertise with flow cytometer instruments and their associated software including AI tools.
• A diverse skillset in bioanalytical assay techniques such as cell culture, cell imaging, ligand binding, receptor occupancy or enzyme activity assays.
• Outstanding written and oral communication skills along with the ability to work collaboratively in a team setting.
• Demonstrated knowledge and skills in solving scientific problems, ability to troubleshoot.
• Proven ability to lead teams and direct the work of staff members at all levels.

Preferred Qualifications:

• Experience ​in immunology.
• Demonstrated experience in complex immunophenotyping assay development and implementation in clinical trials in line with industry's best practices and current regulatory expectations for validation of flow cytometry assays.
• Experience working with a laboratory information system, such as Watson LIMS, to manage sample tracking and data analysis.
• Experience using an electronic laboratory notebook.
• Knowledge of biological sample collection techniques and their suitability for different types of analysis.
• Experience validating software and equipment in a regulated laboratory setting.
• Experience in implementation of a variety of methods, such as ligand binding or mass spectrometry, in a regulated setting.
• Experience working with Quality Assurance in a compliance-related environment.
• Knowledge of requirements for working in a regulated environment (GLP, GCLP, CLIA) in support of nonclinical and/or clinical development projects.
• Exposure to working with Quality teams in a GxP environment.
• Experience supporting regulatory filings.
• Experience with clinical trial operations.

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.