Global Trial Lead (multiple openings)

Role: The Global Trial Lead (GTL) holds full operational accountability for end-to-end execution of global medical studies across all phases, ensuring timely delivery, budget adherence, and regulatory compliance. Responsibilities include managing clinical trial operations, overseeing vendor and CRO performance, developing and implementing operational standards, risk management, and maintaining study documentation in systems like Veeva. The GTL collaborates closely with the MEG Lead and cross-functional teams on study planning, budgeting, resource allocation, and issue resolution. Qualifications: Requires a BA/BS, with a minimum of 4 years in clinical/medical operations, project management, and global trial experience within the pharmaceutical or healthcare sector. Demonstrated expertise in managing multi-national studies, vendor relationships, and regulatory standards (GxP, GCP). Preferred skills include experience with CRO management, study lifecycle oversight, and familiarity with clinical systems like CTMS. HighValue: Global trials, study phases from start-up to closeout, therapeutic area experience preferred, vendor and budget management, GxP compliance, cross-functional leadership, up to 25% travel. WorkSetup: Location not specified, role involves global collaboration.