Global Medical Information Strategy Lead

Revolution Medicines; United States; Sur place; USD 177 000 - 221 000; Plein temps

Résumé du poste

Revolution Medicines is seeking an Associate Director of Medical Information to lead timely, accurate scientific responses for HCPs, patients, and caregivers. You will develop content, support information resources, and manage inquiries across the product lifecycle.

The role requires a strong scientific background, experience in Medical Information within pharma/biotech, and the ability to work in a dynamic environment with cross-functional teams. Travel ~10–20% may be required.

Qualifications

• Advanced degree in a scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
• Experience supporting Medical Information activities within the pharmaceutical or biotechnology industry, including familiarity with regulatory and compliance requirements.
• Excellent verbal and written communication skills.
• Experience creating, reviewing and managing scientific content for diverse audience.
• Strong organizational, problem-solving and project management skills.
• Demonstrated ability to collaborate effectively with cross-functional stakeholders and external partners.
• Self-motivated, with the ability to exercise sound judgment, work with appropriate autonomy, and adapt to changing priorities.
• Proficiency in medical information databases, content management systems and other relevant software tools.
• Experience with Veeva PromoMats preferred.
• Willingness to travel, approximately 10-20%.

Responsabilités

• Develops, reviews and maintains Medical Information resources, including standard response documents (SRDs), custom response letters (CRLs), FAQs and other approved response materials.
• Ensures all Medical Information content is scientifically accurate, evidence-based, consistent with the latest clinical data, and compliant with applicable regulatory requirements, industry codes and medical information standards.
• Supports the management of unsolicited inquiries from healthcare professionals, patients and caregivers, ensuring responses are accurate, compliant and timely.
• Monitors and analyzes Medical Information inquiry trends and customer insights to identify emerging scientific information needs, inform content development, and recommend operational improvements.
• Provides Medical Information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across relevant stakeholders.
• Supports Medical Information activities at scientific congresses, including preparation of congress-specific Medical Information resources and staffing Medical Information booths.
• Contributes to the development, implementation, and maintenance of Medical Information SOPs, work instructions, and operational processes to support compliance with applicable regulatory requirements, industry standards, and company policies.
• Monitors relevant scientific publications and clinical trial data to inform Medical Information content and strategy.
• Partner cross-functionally with Medical Affairs, Clinical Development, Regulatory, Legal/Compliance, Safety, Commercial, and other stakeholders to support launch readiness and product lifecycle needs.
• Provides Medical Information expertise and support for additional Medical Affairs initiatives and projects as needed.

Connaissances

Advanced degree in science/medicine

Cross-functional collaboration

Project management

Excellent communication

Medical information experience

Regulatory/compliance knowledge

Proficiency with medical information/;

Willingness to travel

Formation

Advanced degree in scientific/medical discipline

PharmD/MD/PhD preferred

Outils

Veeva PromoMats

Description du poste

Revolution Medicines is seeking an Associate Director of Medical Information to lead timely, accurate scientific responses for HCPs, patients, and caregivers. You will develop content, support information resources, and manage inquiries across the product lifecycle.

The role requires a strong scientific background, experience in Medical Information within pharma/biotech, and the ability to work in a dynamic environment with cross-functional teams. Travel ~10–20% may be required.