Senior, Global Trial Lead
Hyderabad, INPosted Jul 17, 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 LeadHyderabad - TS - INApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Duties/ResponsibilitiesResponsibilities 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 Leads 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 May support the development of others within the department and/or enterpriseBudgeting & Resource Planning Drives upfront planning of study timelines and budgets in partnership with cross-functional...