Head of Medical Information

Bristol Myers Squibb; United States; Vor Ort; USD 180.000 - 240.000; Vollzeit

Benefits dieser Stelle

Remote work

Up to 25% travel

Zusammenfassung

RayzeBio is seeking a Head of Medical Information within its Medical Affairs organization, focusing on disseminating scientific and clinical information for oncology radiopharmaceuticals. You will shape the information strategy and oversee lifecycle management of medical content.

The role requires an advanced medical degree with 5–8 years in Medical Information or Medical Affairs, plus oncology/radiopharmaceutical expertise and strong regulatory knowledge.

Qualifikationen

• Advanced professional degree in the sciences (PharmD/PhD/MD).
• 5–8 years in Medical Information or Medical Affairs.
• Expertise in oncology and radiopharmaceuticals.
• Knowledge of industry compliance/regulations.
• Strong project management and communication abilities.

Aufgaben

• Develop medical information strategy.
• Oversee content lifecycle management (FAQs, slide decks).
• Train call center/vendor teams.
• Ensure compliance through MLR review.
• Liaise with Bristol Myers Squibb to align practices.
• Support medical insights, congress presence, and market access activities.

Kenntnisse

Medical information strategy

Oncology

Radiopharmaceuticals

Regulatory compliance

Project management

Communication

Vendor management

Ausbildung

PharmD/PhD/MD

Jobbeschreibung

Role:

Head of Medical Information supporting RayzeBio's Medical Affairs, focusing on scientific and clinical information dissemination for oncology radiopharmaceuticals.

Responsibilities:

• develop medical information strategy
• oversee content lifecycle management (FAQs, slide decks)
• train call center/vendor teams
• ensure compliance through MLR review
• serve as a liaison with Bristol Myers Squibb to align practices
• also supports medical insights, congress presence, and market access activities

Requirements:

• advanced scientific degree (PharmD, PhD, MD)
• 5–8 years' experience in Medical Information or Medical Affairs
• expertise in oncology and radiopharmaceuticals
• knowledge of industry compliance/regulations
• strong project management
• communication skills

Preferred:

• experience with Radiopharmaceuticals Targeting Solid Tumors
• supporting content development and vendor oversight

High-Value:

• Oncology
• radiopharmaceutical modality
• focus on solid tumor targets
• support for scientific and promotional materials
• MLR review
• leveraging AI for content and program optimization

Location:

remote with travel up to 25%, preferred in San Diego or Princeton.