Erasca
SVP Late Clinical Development
San Diego, CA or remote
Sponsorship not specified$400k-$465kDetected 56 days ago
Business DevelopmentClinical TrialsClinical ResearchPharmacovigilanceResearchLeadershipCommunicationCollaborationWriting
About the role
- 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 anticipated salary range for this position is $400,000 to $465,000.
- The final salary offered to a <span class="Nor
Responsibilities
- Lead late clinical development function, directly and through reports.
- Design and implement novel and efficient registration enabling clinical trials to assess appropriate endpoints.
- Contribute to regulatory filings including authoring clinical sections for NDAs and other related documents.
- Partner with Drug Safety to assess the safety profile of compounds.
- Contribute to the development and review of scientific publications; author manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectives.
- Recruit, retain, and develop high-functioning late clinical development team.
- Establish, develop, and maintain relationships across Erasca, particularly with partners and stakeholders in Research and Development.
- Perform all duties in keeping with the Company's core values, policies and all applicable regulations.
- Demonstrated ability to collaborate successfully with multiple functions in a matrixed team environment.
- Demonstrated ability to achieve high performance goals and meet deadlines in a fast-paced environment; a collaborative team player with a can-do attitude and the ability to identify and implement creative solutions to complex problems.
Requirements
- M.D. degree or equivalent, with subspecialty fellowship training and board certification or eligibility in Oncology or Oncology/Hematology.
- Experience as the clinical lead on complicated global programs with multiple indications and studies required.
Nice to have
- Experience with product launch and commercialization highly preferred.
- Experience in early development a plus.
- 12+ years of oncology clinical trial and drug development experience, including extensive experience in the pharmaceutical or biotechnology industry.
- The ideal candidate will bring a combination of clinical practice, academic clinical trials, and industry experience, with both large and small company experience a plus.
Compensation
- The anticipated salary range for this position is $400,000 to $465,000.
Benefits
- Direct management of medical and scientific staff in clinical development required; experience leading medical affairs function highly preferred.
- Experience leading or being closely involved in the clinical aspects of a regulatory filing and direct interaction with health authorities required.
- Strong learning orientation, curiosity, and commitment to science and patients.
- Provide medical direction and high-quality scientific and clinical knowledge to guide the strategy and execution of late-stage clinical programs and contribute to clinical decision making across the Erasca portfolio.
- Serve as Medical lead on clinical programs and r epresent Clinical Development on program teams.
- In collaboration with head of Medical Affairs, continue the establishment and execution of medical affairs strategy and tactics.
- Write medical aspects of core study and regulatory documents including clinical research plans, protocols, investigator brochures, clinical study reports and regulatory submissions.
- Present at scientific, medical, and regulatory meetings.
- Required Education and Experience:
This listing is sourced directly from Erasca's careers page and normalized into a canonical job model.