Global Medical Affairs Director – Oncology
Sanofi
Global Medical 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
- Co-build, develop and lead the execution of the medical strategy for assigned assets in our pipeline across the product value chain, from First in Humans use (M2 stage) to loss of exclusivity
- Exert 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
- 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: 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 assets moving into Ph3 and onwards
- Oversee the design of key medical programs/initiatives to drive the therapeutic value of our assets 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
- Deep expertise in Oncology
- 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
- Education: Doctorate in relevant scientific discipline or Pharmacy – Medical Degree preferred
- Minimum 2 years of experience in relevant Medical Affairs, MSL, or Therapeutic Area capacity
- 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
Oncologyclinical trials managementevidence generationscientific communicationdrug developmentregulatory knowledgemarket accessreimbursementmedical strategyIntegrated Patient Journey (IPJ)
Soft skills
cross-functional leadershiptrust buildingstrategic inputtransversal collaborationinsight generationexecution planningbudget managementalignment with strategycommunicationteam leadership
Certifications
Doctorate in relevant scientific disciplinePharmacy – Medical Degree