The Opportunity
We are seeking a dynamic medical leader with a background in disciplines related to cardiovascular, renal, and metabolism (CVRM) to join the Medical network at Genentech. The Principal Medical Director will provide exceptional clinical and scientific leadership for medical affairs activities in the area of CVRM and related disorders, aiming to generate and communicate medical evidence that aids practitioners, patients, and payers in making informed health care decisions. The successful candidate will exhibit outstanding communication and leadership skills, building strong relationships with key stakeholders internally and externally. This role requires representing the US Medical function within cross-functional teams and initiatives at Genentech, Roche’s global organization, and external customer engagements, with an emphasis on leading fit-for-purpose teams, prioritizing work flexibly, and engaging in partnerships to address complex multidisciplinary challenges.
Key Responsibilities
Clarify and communicate medical perspective to a broader network of Medical Affairs professionals in both home and field organizations.
Compile, analyze, and interpret complex datasets from internal and external sources and provide recommendations to CMG and PD teams to support critical decision making for asset development programs
Propose clinical and medical strategies that lead to optimal evidence generation and launch readiness in the US
Design, execute, and monitor plans, and tactics throughout the product lifecycle.
Represent Genentech Medical Affairs externally at key meetings.
Develop scientific partnerships with therapeutic area experts and execute collaborations.
Lead efficient implementation of medical tactics by leveraging relevant expertise and insights.
Execute US Medical/global clinical trial activities conducted as part of Medical Affairs.
Who you are
Qualifications & Experience
Advanced Clinical/Science Degree required (MD)
Minimum 8-10 years of relevant clinical / medical pharmaceutical/biotechnology industry experience with knowledge of CVRM development and reimbursement landscapes
Experience or relevant knowledge of pre-approval drug development trials and post marketing medical evidence generation, including expertise in controlled and observational study designs, data analysis, and clinical/health economic interpretations
Understanding of the US health care environment including the payer landscape, evidence based medicine tools and practices, and health technology assessments
Ability to navigate complex and challenging situations and flex and thrive in an ambiguous environment.
Location/ Travel Requirements
The position is located in South San Francisco. The position may require up to an additional 35% time traveling.
The expected salary range for this position based on the primary location of South San Francisco, CA is $277,800 - 515,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Relocation benefits are not available for this job posting.
