8 дней назад
US Senior Medical Director, Rare Hematology
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
US Senior Medical Director, Rare Hematology (Rare Hematology/Medical Affairs): Developing and executing U.S. medical strategies across a rare hematology portfolio, including ITP, wAIHA, and SCD, with an accent on launch readiness, clinical evidence, and cross-functional leadership. Focus on leading investigator-sponsored studies, scientific communications, MSL direction, payer engagement, and compliant medical support for rilzabrutinib.
Location: Cambridge, Massachusetts, or Morristown, New Jersey, United States; onsite and approximately 20% travel required
Company
is a global healthcare and biopharmaceutical company developing treatments for immune challenges, rare diseases, blood disorders, cancers, and neurological conditions.
What you will do
- Develop U.S. medical objectives and strategies across the rare hematology portfolio, aligned with commercial goals.
- Serve as the internal expert for rare hematologic conditions and products, supporting the U.S. Medical Affairs field team.
- Lead medical advisory boards, investigator-sponsored studies, scientific communication, and publication strategies.
- Partner with R&D to support clinical trials and lead medical affairs activities for the rilzabrutinib launch in ITP.
- Direct disease-specific MSL teams and provide product and disease-state training to internal colleagues.
- Support payer discussions, educational grants, promotional and medical review, and compliance across Medical Affairs activities.
Requirements
- Doctorate degree in PhD or PharmD; MD candidates with relevant experience will be considered.
- At least 10 years of Medical Affairs experience involving strategic and tactical planning and execution.
- Experience in rare hematology or a related area, such as ITP, wAIHA, SCD, or adjacent rare blood disorders.
- Strong strategic planning, communication, presentation, interpersonal, and conflict-resolution skills.
- Ability to work effectively in a highly matrixed, cross-functional environment.
- Commitment to ethical, legal, regulatory, and scientific standards.
Nice to have
- Experience developing, conducting, and publishing peer-reviewed scientific or clinical research.
- Additional training or experience in epidemiology, health economics, health policy, or outcomes-based research and practice.
Culture & Benefits
- Work alongside a supportive, future-focused team in a science-driven healthcare environment.
- Opportunities for professional growth through promotion or lateral and international moves.
- Health and wellbeing benefits, including healthcare, prevention, and wellness programs.
- At least 14 weeks of gender-neutral parental leave.
- Rewards and benefits designed to recognize contribution and impact.
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