Erasca is a clinical-stage precision oncology company driven by a bold mission—to erase cancer. Backed by a16z.
About the role
Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide.
What they're looking for
- Experience as the clinical lead on late-stage clinical programs in lung cancer highly preferred
- Experience leading or being closely involved in the clinical aspects of a regulatory filing and direct interaction with health authorities required
- Exposure to early development and the transition from FIH to registrational trials preferred
- Extensive knowledge of clinical trial methodology and the regulatory and compliance requirements governing clinical trials
- Demonstrated ability to collaborate successfully with multiple functions in a matrixed team environment
- Executive leadership skills to educate and influence stakeholders and to add value in strategic business planning and decision-making
More about this role
Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer.
Reporting to the Chief Medical Officer, the VP Clinical Development and Global Program Lead (GPL) for Lung Cancer will provide medical leadership and oversight of the lung cancer development program and collaborate with the CMO across the Erasca portfolio. Responsibilities will include clinical development strategy, protocol development, registrational strategy and execution, KOL and academic site interactions, competitive landscape diligence, presentation of data, and other clinical deliverables. In addition, the VP will be a hands–on drug developer and will serve as clinical lead and/or medical monitor on individual studies.
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