Global Medical Affairs Senior Director – Gastroenterology
| Company | Sanofi |
|---|---|
| Location | Cambridge, MA, USA, Morristown, NJ, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | MD |
| Experience Level | Senior, Expert or higher |
Requirements
- MD required.
- Minimum 8 years’ experience in Academia and/or industry.
- Strong understanding of the pharmaceutical/biotech drug development and commercialization process.
- Excellent communication and presentation skills with the ability to present scientific data in a credible manner.
- Highest integrity; committed to ethics and scientific standards.
- Able to influence and work on projects in collaboration with our partners and establish excellent working relationships and credibility.
- Able to interface professionally with a wide spectrum of internal and external academicians, agencies, and industry executives in the scientific/medical arena.
- Personal style that includes a sense of urgency, as well as flexibility and ability to respond to rapidly changing environments and circumstances.
- Active listening, collaborative and proactive, with a hands-on, roll-up-the sleeves style and attitude.
Responsibilities
- Support the Head of Global Medical Affairs Dupilumab Rhinology and Gastroenterology in the build and execution of Global Med Affairs strategy.
- Build and execute the Life Cycle management for Dupilumab Gastroenterology including pediatric indication; define and prioritize the future needs including new study ideas and tactics to prioritize the best areas for clinical trial investment.
- Collaborate with alliance partners at Regeneron: take a team-oriented approach to making sure strategy is clearly defined and consistent with relevant stakeholders in clinical development and commercial teams.
- Coordinate data gap analyses across the Regions and countries.
- Establish IEGP plans and supervise the implementation.
- Collaborate with the Alliance to execute the data generation activities in alignment with the Brand plan and Global Medical Affairs Plan.
- Lead and supervise analyses from the development program dupilumab for additional publications.
- Guide physician/scientist in charge of the execution of the GMA LCM and data generation.
- Establish and maintain strong relationships with experts in the Gastroenterology field, academics and professionals, medical/scientific organizations, and patient associations.
- Lead advisory boards or roundtables for anti-IL-4/IL-13 in Gastroenterology and gain strategic insights for medical, scientific, and development strategy.
- Give significant input to publications and co-author relevant abstracts. Drive process of data dissemination and ensure that it is publicly presented in an appropriate and timely fashion and in a fair and balanced manner.
- Ensure the scientific integrity of sponsored and supported research, information, and relationships with healthcare providers and patient advocacy groups.
- Ensure a data-driven patient-centric approach to development of medical strategy both for product and device development as well as possible services which can enhance the value proposition of the product; Provide relevant feedback to market access teams to ensure optimal pricing and reimbursement strategy and inclusion of relevant endpoints in clinical trials.
- Travel required, comprising approximately 30%.
Preferred Qualifications
- Prior experience in a Global or at minimum Regional medical affairs role. Global experience highly advantageous.
- Prior experience in Immunology/Immune Inflammation Medical Affairs Life Cycle management.
- Experience working within an international/global company with a complex organizational environment; able to operate in a matrix team-oriented structure.
- Experience in Medical Affairs with Biologics (Dermatology, Rheumatology, Gastro others.) highly advantageous.