Associate Director, Global Trial Lead
Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb (BMS)
Job Type: Full-time (Hybrid – Site-by-Design)
About Bristol Myers Squibb (BMS)
At Bristol Myers Squibb, we’re driven by a single vision — Transforming patients’ lives through science™. Every role here is meaningful and contributes to improving global health outcomes. Whether optimizing manufacturing processes or leading global clinical programs, you’ll work on projects that are both challenging and life-changing.
BMS promotes flexibility, career growth, and well-being through a variety of benefits, programs, and development opportunities.
Learn more: careers.bms.com/working-with-us
Position Overview
As an Associate Director, Global Trial Lead (GTL), you will lead the strategic planning, execution, and oversight of global clinical trials across multiple therapeutic areas. You’ll drive operational excellence, vendor performance, risk mitigation, and ensure studies are delivered on time, within budget, and to the highest quality standards.
Key Responsibilities
1. Project Management
Lead collaboration between internal study teams and external vendors to ensure successful trial execution.
Provide strategic input on study feasibility, site selection, and operational planning.
Proactively manage risks, timelines, budgets, and quality deliverables.
Oversee and manage CRO and vendor SOWs, ensuring alignment with contracts and performance expectations.
Review and approve vendor invoices, accruals, and scope amendments.
Monitor progress through performance metrics and quality indicators.
Maintain study data in Veeva systems (CTMS, eTMF).
Develop and maintain project management tools (action logs, decision trackers, issue logs, risk plans).
Lead implementation of cross-functional best practices and promote operational consistency across programs.
2. Study Input & Strategic Guidance
Provide therapeutic and operational insights for study protocol design and execution.
Advise cross-functional teams on risk mitigation and process improvement.
Mentor junior GDO Study Team members and support departmental skill development.
Identify and apply trends in clinical operations to enhance trial strategy.
3. Budgeting & Resource Planning
Lead study-level budgeting and forecasting, partnering with cross-functional teams.
Manage vendor logistics and resourcing needs across global programs.
Conduct quarterly budget reviews and report variances to finance.
Ensure financial efficiency and accuracy throughout the trial lifecycle.
4. Program & Study Oversight
Oversee strategic planning and operational execution of multiple global trials from start-up through close-out.
Lead cross-functional Study Teams to ensure alignment with franchise goals and regulatory compliance.
Drive continuous process optimization using data-driven insights.
Build and maintain partnerships with internal (Clinical Research, Affiliates) and external (CROs, AROs) stakeholders.
Contribute to portfolio-level operational excellence initiatives.
Core Competencies
Technical Expertise
Global Trial & Project Management: Proven leadership in end-to-end clinical trial execution and regulatory compliance.
Operational & Budget Oversight: Expertise in managing trial operations, vendors, timelines, and budgets.
Risk & Quality Management: Strong focus on GCP/GXP adherence and audit readiness.
Stakeholder Engagement: Skilled at managing global cross-functional teams and vendor partnerships.
Clinical & Regulatory Knowledge: Deep understanding of trial phases, submission processes, and global standards.
Systems & Data Management: Proficient in CTMS, eTMF, and other trial management systems.
Leadership Competencies
Leadership & Collaboration: Fosters teamwork, inclusivity, and shared accountability.
Critical Thinking & Decision-Making: Balances risks, cost, and patient safety in complex decision contexts.
Accountability & Results Focus: Delivers projects on time, within scope, and to quality expectations.
Adaptability & Resilience: Maintains composure and drives solutions amid change or uncertainty.
Communication & Relationship Building: Effectively engages with diverse, global stakeholders.
Qualifications
Education
Bachelor’s degree (BA/BS) in a relevant scientific discipline — Required
Advanced degree — Preferred
Experience
Minimum 7 years of experience in clinical operations, project management, or related pharmaceutical/healthcare functions.
Proven track record leading complex global clinical trials independently.
Experience managing cross-functional, multinational teams.
Prior experience managing CROs and external partners preferred.
Travel requirement: Up to 25%
Work Environment
Occupancy Type: Site-by-Design — minimum 50% onsite presence at assigned facility.
Hybrid flexibility for collaboration, innovation, and productivity.
Equal Employment Opportunity
BMS is committed to creating an inclusive workplace that values diversity. We provide reasonable accommodations for applicants and employees with disabilities.
Learn more: careers.bms.com/eeo-accessibility
Additional Information
COVID-19 vaccination strongly recommended.
Applicants with arrest or conviction records will be considered in accordance with local laws.
Data privacy and recruitment processes comply with all applicable global regulations.
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