Scientific / Medical Director, Global Hematology Pipeline, Medical Affairs

Scientific/Medical Director, Global Hematology Pipeline, Medical Affairs

Responsibilities:
- Support creation and execution of disease and asset strategies.
- Support pipeline medical evidence generation strategy and execution (company-sponsored studies, research collaborations, investigator-initiated studies).
- Lead creation of early scientific narratives, messaging, and communications activities (congress planning, medical education, publication strategies/plans).
- Provide in-house medical expertise; coordinate scientific activities with internal/external stakeholders; may participate in due diligence/business development; contribute to translational strategy with discovery.
- Act as medical interface; develop and execute medical expert engagement strategies; partner with clinical development, commercial, access, area, and affiliate colleagues.
- Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members; stay current via conferences/literature.
- Assist in development of medical education programs, advisories, symposia; review/develop/approve/execute/communicate affiliate/area/global medical affairs-sponsored or supported clinical research.
- Coordinate scientific/medical activities with internal stakeholders (commercial, clinical operations, discovery, statistics, regulatory); serve as scientific team interface for key regulatory discussions.
- Ensure budgets, timelines, and compliance requirements are factored into scientific activities.

Qualifications:
Scientific Director:
- PhD or PharmD; additional post-doctorate experience highly preferred.
- 5–7+ years pharmaceutical industry experience.
- 7–10 years Medical Affairs with Global Medical Affairs experience highly preferred.
- Multiple myeloma and cell therapies experience highly preferred.
- Knowledge of clinical trial methodology, data analysis/interpretation, regulatory requirements; experience in development strategy and protocol design.
- Proven leadership in cross-functional global teams.
- Excellent oral/written English communication.

Medical Director:
- MD (or equivalent: DO or non-US M.D.); relevant academic/hospital specialty preferred; residency/fellowship preferred.
- 0–2 years clinical trial/medical affairs experience; 3+ years preferred.
- Multiple myeloma and cell therapies experience highly preferred.
- Knowledge of clinical trial methodology, data analysis/interpretation, regulatory requirements; experience in development strategy and protocol design.
- Proven leadership in cross-functional global teams.
- Ability to interact externally/internally to support global business strategy.
- Excellent oral/written English communication.