Senior Medical (Science) Director, Lung Cancer

About the role

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

The Sr. Medical Science Director/Sr. Medical Director at Genentech puts patients and science at the center of all actions. They drive medical tactics aimed at maximizing medical progress for patients. They collaborate to drive timely data generation and dissemination.

They are expected to maintain an in-depth understanding of the medical strategy and relevant clinical and payer issues, while ensuring Genentech's partners understand key trends and shifts in the external healthcare landscape. They serve as the guardian for high standards of compliance, ethics and safety. This role is organized within a network of experts, and therefore may be performing a variety of medical activities, as needed.

The Opportunity

The Sr. Medical Science Director/ Sr. Medical Director will provide exceptional clinical and scientific leadership for medical affairs activities, aiming to generate and communicate medical evidence that aids practitioners, patients, and payers in making informed health care decisions. The successful candidate exhibits outstanding communication and leadership skills and builds strong relationships with key stakeholders.

This position will also represent the US Medical function within cross functional teams and initiatives at Genentech, within the Roche global organization, and in external customer facing engagements. In addition to strong communication skills, this position requires the ability to lead fit-for-purpose teams in a matrix environment, flexibility in prioritizing work, and a mindset to engage in purposeful partnerships to solve complex multi-disciplinary challenges.

Key Responsibilities

• Design, execute, and monitor medical strategies, plans and tactics spanning the lifecycle
• Provide clinically meaningful perspective for regulatory and other scientific communications
• Clinical Study Design and Management
• Scientific Engagement with Genentech's Internal and External Stakeholders:
• Congress Planning and Medical/Scientific Content Communications & Review:
• Accountable for implementing strategy through medical tactics, tapping into the network of relevant expertise and insights
• Maintaining an in-depth understanding of relevant medical strategy and clinical, patient/caregiver, payer and healthcare/market landscape
• Act as a guardian for high standards of compliance, ethics and safety; putting patients at the center of all actions.

Required Qualifications & Experience

• Advanced Clinical/Science Degree required (e.g. PharmD, PhD, MD etc.)
• Minimum 8+ years of relevant biopharmaceutical industry experience.
• Understanding of and/or previous experience with Phase I - III and/or Phase IV drug development
• Considerable experience across Medical Affairs domains including: principles and techniques of data analysis, data interpretation and assessment of clinical relevance, medical writing and reviewing, medical strategy development, external engagement planning and execution, etc.
• Experience or relevant knowledge of pre-approval drug development trials and/or 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, marketplace factors/dynamics, evidence-based medicine tools and practices, etc.
• Proven record in developing strong relationships with external stakeholders (therapeutic area experts, external organizations, etc.)
• Great team player; Highly collaborative; Good interpersonal and influencing skills; Can effectively and quickly establish rapport and influence without authority

Preferred Experience

• Expertise and industry experience in the therapeutic area
• Experience with data strategy, digital platforms (Adobe, Veeva, Salesforce), user research, and clinical trial recruitment tactics

Location / Travel Requirements

The position is located in South San Francisco. The position may require up to an additional 35% time traveling.

Pay and benefits

The expected salary range for this position based on the primary location of South San Francisco, CA is $198,600 - 471,000. 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.

Benefits

• Relocation benefits are not available for this job posting.
• If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.