Sr. Manager, Study Start Up

Role: Senior Manager, Study Start-up, leads global clinical trial initiation and site activation for Phase I-III and real-world evidence studies. Responsibilities: oversee end-to-end study start-up activities, develop strategic plans, partner with CROs, streamline processes, analyze trial data for forecasting, and ensure timely site activation within regulatory and operational standards. Collaborates with internal teams, external vendors, KOLs, and CROs to enhance efficiency and ensure high-quality delivery. Qualifications: Bachelor’s in Science or related field; 8+ years’ experience with CRO or biopharma in multinational studies; 5+ years managing clinical operations, particularly study start-up and site activation. HighValue: extensive experience with CRO collaboration, global site activation, GCP compliance, and clinical trial conduct across phases; expertise in feasibility, country/site selection, and patient recruitment. WorkSetup: not specified; likely hybrid or onsite, based on industry standards.