Erasca, Inc.

• Provide medical leadership and oversight for pancreatic and colorectal cancer development programs
• Collaborate with the Chief Medical Officer across the Erasca portfolio
• Lead the clinical development subteam for all GI cancer studies
• Design and implement novel, efficient clinical trials and assess appropriate endpoints
• Lead clinical study subteams and monitor study integrity
• Review, interpret, and communicate safety and efficacy data
• Develop registrational strategies and contribute to regulatory filings and health authority interactions
• Author clinical sections for INDs, NDAs, and related documents
• Serve as medical lead and/or medical monitor on clinical programs and individual studies
• Partner with Drug Safety to assess compound safety profiles
• Author or support medical aspects of clinical research plans, protocols, investigator brochures, clinical study reports, and regulatory submissions
• Contribute to scientific publications and author manuscripts
• Present at scientific, medical, and regulatory meetings
• Maintain clinical and scientific expertise through literature review and engagement with thought leaders, investigators, stakeholders, and partners
• Participate in due diligence and business development activities
• Hire, develop, and mentor medical directors and clinical scientists
• Establish and maintain relationships across Erasca, particularly with Research and Development partners and stakeholders
• Perform duties in accordance with company values, policies, and applicable regulations

SVP Clinical Development – Global Program Lead, Pancreatic Cancer