Manager Study Start Up

Role: Manage feasibility, site agreements, and study start-up activities for Summit’s global Phase 3 oncology clinical trials, including NSCLC and CRC indications. Responsibilities: negotiate site contracts/budgets, support site activation, coordinate with legal, finance, CROs, and internal teams; develop and implement process improvements; provide status updates and financial forecasts; ensure compliance with GxP, GCP, and regulatory standards; build relationships with external vendors and sites; oversee contract execution and issue resolution. Requirements: 5-7+ years in clinical trial site management, feasibility, and start-up in biotech/pharma; strong knowledge of ICH/GCP, global trial conduct, and contract negotiation; degree in Life Sciences, Business, or related field preferred; proficient in MS Office, electronic document systems, and budget management. Preferred: experience with global multi-site trials, negotiation skills, and financial acumen. HighValue: Oncology (NSCLC, CRC), Phase 3, site feasibility, contract negotiation, global trial experience, GxP/GCP compliance, cross-functional collaboration, budget oversight. WorkSetup: Not specified, likely office-based with potential for remote elements.