The Principal Medical Director plays a pivotal role in guiding clinical and scientific initiatives within the CVRM therapeutic domain. This position entails the formulation of medical strategies, evidence generation, and fostering relationships with essential stakeholders to facilitate informed decisions in healthcare. Applicants should possess an advanced clinical or scientific degree (MD) and have a minimum of 8-10 years of pertinent experience in the pharmaceutical or biotechnology sectors. A strong background in CVRM development, clinical trial design, as well as a thorough understanding of the US healthcare and payer ecosystem is essential.
Genentech provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
