Revolution Medicines is seeking a Director of Medical Information to oversee the creation and management of medical information content, support compendia and submissions, and contribute to AMCP dossier development and review. The ideal candidate is a skilled communicator with a strong scientific background and can manage projects in a dynamic environment.
Requirements
- Develops, reviews and maintains medical information resources such as standard response letters (SRLs), custom response letters (CRLs), FAQs and inquiry response guidance documents
- Manages unsolicited medical information inquiries and partners with the Medical Information call center vendor to ensure accurate, compliant, and timely responses
- Ensures all medical information content is evidence-based, consistent, and aligned with the latest scientific and clinical data
- Collaborates with Medical Affairs, Clinical Development, Market Access and other internal stakeholders to inform scientific communication, guideline strategy, and payer-facing materials
- Supports NCCN guideline submission package development including submission planning and coordination across disease areas
- Leads or contributes to the development, review and maintenance of AMCP dossiers to support market access and payer engagement strategies
- Leads the development and execution of compendia submission process for Medical Affairs
- Serves as Medical Reviewer in the Medical, Legal and Regulatory (MLR) process, ensuring that materials support evidence-based communication and comply with company policies, industry standards, and regulatory requirements
- Collaborates with cross-functional partners to provide strategic medical insights and ensure scientific accuracy in promotional and non-promotional materials
- Provides medical information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across stakeholders
- Provides Medical Information support for congresses, including staffing Medical Information booths and responding to HCP inquiries
- Leads the development and maintenance of internal SOPs and processes to ensure compliance with regulatory requirements and industry standards
- Demonstrated success leading cross-functional medical information strategies that influence scientific communication, market access, and global readiness
- Monitors relevant scientific publications and clinical trial data to inform medical information content and strategy
- Provides support for other Medical Affairs projects as needed
Benefits
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities
