Senior Global Trial Lead

Warsaw, PolandPosted Jul 9, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsSenior Global Trial LeadWarsaw - PL No longer accepting applications.Job IDR1600550Date posted03/16/2026DepartmentClinical Trial ManagementPosition Summary The Global Trial Lead (GTL) provides strategic and operational oversight for global clinical trials, ensuring they are executed with excellence—on time, within budget, and in compliance with regulatory standards and internal policies. This role serves as a key leader within Global Development Operations (GDO), contributing to study-level strategy, cross-functional alignment, and issue and risk resolution. The individual guides trial execution across all phases and manages relationships with vendors to uphold performance and quality. This role may also lead global initiatives, support Operational Portfolio Leads on asset, trial and/or therapeutic-level inquiries, and influence decision-making at both study and organizational levels. The Global Trial Lead plays a pivotal part in driving delivery of registrational and non-registrational studies, with broad impact across therapeutic areas and global teams. Note: The Global Trial Lead (GTL) role has several levels, activities listed with an * are specific to the AD, GTL role. Key Responsibilities Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to, the following: Project Management • Spearheads collaboration with internal study teams and vendors to ensure clinical trial delivery meets established timelines, budgets, and quality benchmarks. • Provides strategic input on study feasibility and oversees operational activities of internal and external contributors. • Identifies and proactively manages risks, balancing trade-offs between cost, deliverables, and quality. • Manages scope of work (SOW) for CROs and Vendor Partners, ensuring alignment with contractual terms, budgetary targets, and quality standards. • Participates in vendor selection and evaluation processes. • Reviews, approves, and reconciles vendor invoices, accruals, and scope amendments. • Utilizes performance metrics and quality indicators to monitor and optimize trial execution. • Maintains and ensures accurate data records in study management systems such as Veeva (i.e. CTMS, eTMF, etc.) • Develops and enforces trial-specific standards aligned with broader portfolio strategies to promote operational consistency. • Leads development and execution of cross-functional and global best practices. • Establishes and maintains study-level project management tools, including action logs, decision trackers, issue registers, and risk mitigation plans. • Collaborates cross-functionally to ensure timely knowledge and information sharing. Study Input & Strategic Guidance • Offers therapeutic and operational guidance on study protocols and execution strategies. • Provides consultation across programs/studies with a focus on risk mitigation and operational excellence. • Monitors trends in clinical operations and advises teams on proactive responses. • Mentors global GDO Study Team members within assigned therapeutic areas and others, as applicable •...

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