Senior Medical Director, Oncology Clinical Development (GI)

Role: Lead clinical development activities for one or more therapeutic programs, overseeing trial design, execution, and data interpretation to support product strategy. Responsibilities: manage clinical trial planning, ensure study integrity, oversee safety monitoring, and lead scientific reporting for regulatory submissions. Act as a clinical expert within cross-functional teams, contribute to clinical strategy development, and ensure compliance with GCP, regulatory, and quality standards. May supervise Medical and Scientific Directors and participate in business development activities. Qualifications: MD or DO with relevant specialty, minimum 2 years of clinical trial experience in pharma, academia, or equivalent, with strong knowledge of trial methodology, regulatory requirements, and clinical strategy. Must possess excellent communication skills and ability to operate independently within global teams. HighValue: Oncology, immunology, neuroscience; clinical phases Ph1-3; biologics or small molecules; global drug development; regulatory submissions; cross-functional collaboration with Medical Affairs, Discovery, and Commercial units. WorkSetup: Not specified, but implies global and collaborative environment.