Senior, Global Trial Lead

Working with Us Challenging. 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/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   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 enterprise Budgeting & Resource Planning   Drives upfront planning of study timelines and budgets in partnership with cross-functional teams.  Manages program-level vendor logistics and escalates resourcing needs appropriately.  Identifies and resolves issues impacting budget and timeline adherence.  Leads quarterly budget reviews, flagging anticipated variances for assigned trials and collaborating with Finance on forecasting.  Study Oversight Provides lifecycle leadership and oversight from start-up to close-out phases.  Leads cross-functional Study Teams and coordinates with clinical and development departments.  Analyzes operational metrics to optimize study execution and ensure alignment with franchise objectives.  Identifies organizational and procedural challenges, proposing actionable solutions.  Builds and maintains strategic partnerships with internal stakeholders (e.g., Clinical Research, Affiliates) and external collaborators (e.g., CROs, AROs).  Specific Knowledge, Skills, Abilities:    Technical Competencies Global Trial & Project Management  Leads global clinical trials with expertise in planning, execution, and oversight. Ensures regulatory compliance, patient safety, and timely delivery of high-quality data. Drives project outcomes through strategic coordination and progress tracking.  Operational & Budget Oversight  Manages end-to-end trial operations, including site selection, recruitment, vendor coordination, and resource planning. Oversees budgets, forecasts, accruals, and cost optimization to ensure financial accuracy and efficiency.  Risk & Quality Management  Identifies and mitigates risks to ensure trial continuity. Maintains GCP/GXP compliance and supports audit readiness with a strong quality mindset.  Stakeholder & Vendor Engagement  Builds strong relationships with internal and external stakeholders. Manages communications, escalations, and alignment across functions and geographies .  Clinical & Regulatory Expertise  Demonstrates knowledge of clinical trial phases, therapeutic areas, and regulatory requirements. Ensures readiness for submissions and compliance with global standards.  Systems & Data Management  Utilizes CTMS and other clinical systems to track milestones, ensure data quality, and support decision-making. Partners with technical teams to maintain system integrity.  Management Competencies Leadership & Collaboration  Drives cross-functional teams toward shared goals. Builds consensus and fosters an inclusive, high-performing culture.  Critical Thinking & Decision Making  Solves complex problems and makes timely, informed decisions that prioritize patient safety and data integrity.  Accountability & Results Focus  Owns outcomes, ensures quality, and delivers on time and within budget through proactive oversight.  Adaptability & Resilience  Responds effectively to change and manages conflict constructively while main