Full-Time

Senior Vice President

Head of Medical Affairs

Posted on 4/21/2024

Revolution Medicines

Revolution Medicines

201-500 employees

Develops precision oncology therapies

Biotechnology

Compensation Overview

$265,000 - $350,000Annually

+ Equity

Senior, Expert

San Carlos, CA, USA

Required Skills
Communications
Requirements
  • Medical Degree: MD or equivalent medical qualification is required. Additional qualifications such as a Ph.D. or M.B.A. would be advantageous.
  • Experience: Minimum of 10 years of progressive experience in medical affairs within the biotech or pharmaceutical industry, with a track record of successful leadership.
  • Therapeutic Area Expertise: Strong knowledge and experience in the specific therapeutic area of focus, including understanding of disease pathology and treatment landscape.
  • Regulatory Acumen: Proven experience in interactions with regulatory agencies, including submissions and approvals.
  • Communication Skills: Excellent communication and presentation skills, with the ability to convey complex medical information to diverse audiences.
  • Leadership Skills: Demonstrated ability to lead and develop high-performing teams, fostering a collaborative and innovative culture.
Responsibilities
  • Medical Strategy: Develop and execute the medical affairs strategy in alignment with corporate goals, ensuring the integration of medical initiatives with clinical development, regulatory affairs, and commercialization efforts.
  • KOL Engagement: Build and nurture relationships with Key Opinion Leaders (KOLs), healthcare professionals, and patient advocacy groups to gather insights, ensure medical education, and enhance the company's reputation in the medical community.
  • Clinical Development Support: Collaborate closely with the clinical development team, providing medical input and guidance throughout the design, execution, and interpretation of clinical trials. Ensure compliance with ethical, regulatory, and scientific standards.
  • Regulatory Affairs Collaboration: Work closely with the regulatory affairs team to provide medical expertise for interactions with regulatory agencies, contribute to regulatory submissions, and ensure adherence to regulatory requirements.
  • Medical Education: Oversee the development and implementation of medical education programs for internal teams, healthcare professionals, and patients. Ensure accurate and timely dissemination of medical information.
  • Real-World Evidence: Drive initiatives to generate and leverage real-world evidence to support product value and safety, collaborating with Health Economics and Outcomes Research (HEOR) teams.
  • Cross-functional Collaboration: Collaborate with cross-functional teams, including commercial, market access, and clinical operations, to integrate medical strategies into broader business plans.
  • Team Leadership: Build and lead a high-performing Medical Affairs team, fostering a culture of collaboration, innovation, and excellence.

Revolution Medicines specializes in developing precision oncology therapies, particularly RAS(ON) inhibitors and RAS Companion inhibitors, with their lead product candidate, RMC-4630, currently in a Phase 1/2 clinical program targeting specific oncogenic mutations in various tumor types. The company's main focus is on developing these therapies to target specific oncogenic mutations in different tumor types, utilizing precision oncology technologies.

Company Stage

IPO

Total Funding

$1.3B

Headquarters

Redwood City, California

Founded

2014

Growth & Insights
Headcount

6 month growth

22%

1 year growth

50%

2 year growth

102%
INACTIVE