Senior Medical (Science) Director, Ophthalmology

Roche • South San Francisco, CA

2d • Remote

About The Position

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. Who you are

Requirements

• 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

Nice To Haves

• Expertise and industry experience in Ophthamology

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees