As an Assistant or Associate Medical Director you will:
Participate in Clinical Development strategy development and present to various internal committees
Provide clinical oversight across all relevant studies and programs
Lead and/or otherwise participate in ongoing clinical study team and relevant sub-team meetings, other interactions and communications
Work with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Support others with clinical science information and input for regulatory submissions and other regulatory processes. Includes developing labeling and packaging language, etc.
Play a role in the development and implementation of communication strategies to support existing and concluded studies. Includes KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
Contribute clinical science input into the relevant therapeutic/disease area scientific strategy. Help research and other Product Development groups to ensure consistency of scientific and late-development strategies with target label claims and corporate goals
Collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in Product Development, research, business development, commercial operations, legal, etc.
We are looking for a professional with 2+ years of clinical trials experience in academic medicine or the biotechnology or pharmaceutical industry with extensive experience in the design, conduct, analysis, and reporting of clinical studies.
In addition you bring:
M.D. degree with board certification or eligibility in Oncology or Hematology/Oncology required
Solid tumor experience, preferably in Breast and/or GI Cancer, as well as experience in or exposure to Cancer Immunotherapy
Exposure to next-generation engineered molecules and doublet and triplet combination study clinical trials will both be advantageous
Significant successful interactions with key opinion leaders and investigators
An excellent scientific track record demonstrated by publication record in peer-reviewed journals
Who We Are
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry
for more than 40 years, using human genetic information to develop novel medicines for serious and
life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious
illnesses. Please take this opportunity to learn about Genentech where we believe that our employees
are our most important asset & are dedicated to remaining a great place to work.
The next step is yours. To apply today, click on the "Apply online" button.
Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.
At Genentech, we share salary ranges with applicants during the recruiting process, if requested. Third party salary estimates may not be accurate or up-to-date.