Lead Medical Director, Product Development, CVRM

The Position

We advance science so that we all have more time with the people we love.

Roche’s Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II – III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The Lead Medical Director makes major contributions to development of the Clinical Development (CD) strategy and plan and is responsible for effective and efficient execution for the assigned molecule(s) / indication(s).

The Opportunity

• You will support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s) / indication(s); gathering and analyzing data and information necessary to create the CD plan; you will participate in the design, development and execution of clinical studies.
• You will act as a medical monitor for assigned studies.
• You will collaborate with a variety of internal / external partners & stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc.
• You may participate in meetings, reviews, discussions and other interactions regarding early development / Phase I studies to provide clinical science input & guidance; including reviewing and providing late stage input to Phase I & II protocols.
• You have a demonstrated understanding of Phase II - III drug development.
• You will take an active role with other Clinical Science Team (CST) members, regulatory and other internal partners / stakeholders in the completion and submission of regulatory filings and other regulatory documentation; you will provide clinical science information and input for regulatory submissions and other regulatory processes.
• You will help support the strategic and operational alignment of the CD plan with the relevant CD strategy, Asset team priorities and goals; you will work with other CST members and relevant sub-teams to develop CD plan components (e.g., analytics / data strategy, KOL development, publications strategy, etc.).

Who You Are : Required

Preferred

This position is based onsite in Boston, MA.

Relocation benefits are being offered for this position.

The expected salary range for this position based on the primary location of Boston, MA is $213,000 - $396,000. 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

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

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.

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