Clinical Research Director

Sanofi

Clinical Research Director at Sanofi leading clinical trial strategy and execution within R&D. Collaborating across functions to drive breakthroughs in immunoscience and AI-powered research.

Posted 7/13/2026full-timeCambridge • Massachusetts, New Jersey • 🇺🇸 United StatesLead💰 $206,250 - $343,750 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical development planning and execution, with a strong focus on regulatory compliance and collaboration across multifunctional teams. Proficient in authoring clinical documents and interpreting study results in the context of Hematology/Oncology.

Highest-signal resume keywords

MD DegreeClinical Development ExperienceHematology/Oncology ExperienceRegulatory ComplianceClinical Document Authoring

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Development PlanningProtocol AuthoringClinical Study Report ContributionScientific Data EvaluationClinical Interpretation of Study Results

Soft Skills

Team CollaborationEffective CommunicationLeadership

Industry Keywords

Regulatory AuthoritiesInformed Consent FormIND/IMPD FilingsNDA/CTDAdvisory Committee Preparation

About the role

Key responsibilities & impact

Establishes or adapts clinical development plan for the program(s) including discussions with clinical investigators, advisors and regulatory authorities and plans contingencies.
Leads, supports and oversees the execution of clinical development and studies activities, including but not limiting to: Authors abbreviated protocol.
Reviews the final protocol and protocol amendments.
Reviews the Informed Consent Form, Written Subject Information and Trial Disclosure Form.
Reviews the study specific committee charters.
Leads study specific committees with operational support.
Leads the clinical interpretation of study results, contributes to clinical study reports and clinical summaries.
Provides effective clinical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine
Participates and contributes to regulatory and safety documents and discussions
Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans
Contributes to the clinical sections of the NDA/CTD, Briefing packages for regulatory meetings, PSP/PIP
Participates in Advisory Committee preparation
Scientific data evaluation and authorship
Authors clinical abstracts, presentations for conferences, and manuscripts, when appropriate
Supports the planning of advisory board meeting. Presents and discusses development strategy and clinical study result with external investigators and advisory boards, as appropriate

Requirements

What you’ll need

MD degree or equivalent
Minimum 3 years industry or academic clinical development experience
Hematology/Oncology experience preferred
Demonstrated ability to work with a multifunctional team to achieve project milestones
Understanding of and willingness to meet applicable regulatory, quality and compliance standards

Benefits

Comp & perks

health insurance
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave