Global Medical Director – Oncology
Sanofi
Global Medical Affairs Director – Oncology
Sanofi
full-time
Posted on:
Location Type: Office
Location: Cambridge • Massachusetts, New Jersey • 🇺🇸 United States
Visit company websiteSalary
💰 $172,500 - $249,166 per year
Job Level
Lead
About the role
- Expert internal cross-functional leadership throughout the GPT-GBT continuum to advance the development of assigned assets, assure successful launches, and follow throughout their life cycle
- Driving Medical Affairs activities for oncology, specifically on clinical evidence generation and implementation therapies
- Build trust with Global external stakeholders to advance their understanding of the therapeutic area and evolve the treatment landscapes for pipeline assets or marketed products
- Co-create the IEGP strategy with Medical Evidence Generation Lead and other evidence generation-related functions for the subcutaneous formulation: Clinical Study Unit (CSU), Real World Evidence (RWE), Health Economics Outcomes Research (HEVA), Medical Operations and Effectiveness (MO&E) and country teams
- Oversee insight generation plan and input to the assigned assets overall medical strategy
- Provide strategic input to Scientific Communications teams to plan and execute evidence dissemination and medical education plans
- Lead the Integrated Patient Journey (IPJ) strategy for subcut globally with Key Markets
- Oversee the design of key medical programs/initiatives to drive the therapeutic value of the subcutaneous formulation and address unmet medical needs (i.e., MAPs, Diagnostic support programs, CSRs, etc)
- Oversee medical tactics and clinical study budgets planning and execution to assure prioritization, alignment with strategy and smart execution
Requirements
- Minimum 2 years of experience in relevant Medical Affairs, MSL, or Therapeutic Area capacity
- Deep expertise in Oncology, strongly preferred
- Expertise in international Device regulation as well as market implementation strongly preferred
- Demonstrated industry experience working in strategic roles from medical affairs or clinical development related areas including scientific KOL engagement, evidence generation and scientific communication at Global and Key Market level, preferred
- Broad drug development experience with robust knowledge of regulatory, market access and reimbursement
- Demonstrated experience in managing clinical trials in a pharmaceutical environment is strongly desired
- Demonstrated specialty care product launch experience at a country level, strongly preferred
- Significant line and matrix management experience, including strong transversal collaboration with key functions such as Research, Clinical Development, Commercial, Health Economics, Value and Access and Product Management functions
- Advanced degree in a scientific discipline (M.D., PhD or PharmD)
- Fluent in English
Benefits
- high-quality healthcare
- prevention and wellness programs
- at least 14 weeks’ gender-neutral parental leave
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
OncologyMedical AffairsClinical Evidence GenerationHealth Economics Outcomes ResearchReal World EvidenceClinical Trials ManagementDrug DevelopmentRegulatory KnowledgeMarket AccessScientific Communication
Soft skills
Cross-functional LeadershipStakeholder EngagementStrategic InputCollaborationTrust BuildingInsight GenerationExecution PlanningTransversal CollaborationCommunicationManagement Experience
Certifications
M.D.PhDPharmD