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Associate Director, Global Trial Lead

7+ years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, Global Trial Lead (GTL)

Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb (BMS)
Travel Requirement: Up to 25%


About Life at BMS

BMS provides challenging, meaningful, and life-changing work that transforms patients’ lives and accelerates careers. Employees engage in uniquely interesting work across all departments, with opportunities for growth, cross-functional collaboration, and innovation.

Work Environment Highlights:

  • Balance and flexibility

  • Competitive benefits and programs supporting professional and personal growth

  • Culture of inclusion, collaboration, and operational excellence

Learn more: BMS Careers


Position Summary

The Global Trial Lead (GTL) provides strategic and operational oversight for global clinical trials, ensuring studies are delivered on time, within budget, and in compliance with regulatory standards.
This role:

  • Contributes to study-level strategy and cross-functional alignment

  • Guides trial execution across all phases

  • Manages vendor relationships to ensure performance and quality

  • Leads global initiatives and supports Operational Portfolio Leads on trial and asset inquiries

  • Mentors GDO team members and influences decision-making at study and organizational levels

Note: Activities marked with * are specific to the Associate Director (AD), GTL level


Key Responsibilities

Project Management

  • Collaborate with internal teams and vendors to ensure trial delivery meets timelines, budgets, and quality standards

  • Provide strategic input on feasibility and oversee operational activities

  • Identify and manage risks, balancing cost, deliverables, and quality

  • Manage scope of work (SOW) for CROs and vendors, ensuring alignment with contracts and budgets

  • Participate in vendor selection and evaluation

  • Review, approve, and reconcile vendor invoices, accruals, and scope amendments

  • Monitor trial execution using performance metrics and quality indicators

  • Maintain accurate study records in systems such as Veeva CTMS, eTMF

  • Develop and enforce trial-specific standards and best practices

Study Input & Strategic Guidance

  • Provide therapeutic and operational guidance on protocols and execution strategies

  • Monitor operational trends and advise teams on proactive solutions

  • Mentor global GDO Study Team members in therapeutic areas

  • Support development of team members across the department

Budgeting & Resource Planning

  • Plan study timelines and budgets in partnership with cross-functional teams

  • Manage program-level vendor logistics and escalate resourcing needs

  • Lead quarterly budget reviews and collaborate with Finance for forecasting

Program & Study Oversight*

  • Oversee multiple clinical trials from start-up to close-out

  • Lead cross-functional Study Teams and coordinate across clinical and development departments

  • Analyze operational metrics to optimize trial execution

  • Build strategic partnerships with internal and external stakeholders


Qualifications & Experience

Education

  • BA/BS or equivalent degree in relevant discipline

Experience

  • Minimum 7 years in clinical operations and project management in pharma/healthcare, including multi-national experience

  • Experience in independently leading complex global clinical trials

  • Experience leading global, cross-functional teams

  • Experience managing CROs is preferred but not mandatory


Knowledge, Skills & Competencies

Technical Competencies

  • Global Trial & Project Management: Planning, execution, oversight, regulatory compliance, patient safety, and data quality

  • Operational & Budget Oversight: Site selection, recruitment, vendor coordination, resource planning, and cost optimization

  • Risk & Quality Management: Risk mitigation, GCP/GXP compliance, audit readiness

  • Stakeholder & Vendor Engagement: Communication, alignment, escalation management

  • Clinical & Regulatory Expertise: Knowledge of clinical trial phases, therapeutic areas, and global regulatory requirements

  • Systems & Data Management: CTMS and clinical systems utilization for tracking and decision-making

Management Competencies

  • Leadership & Collaboration: Build consensus, foster high-performing teams

  • Critical Thinking & Decision Making: Solve complex problems and make informed decisions

  • Accountability & Results Focus: Deliver quality outcomes on time and within budget

  • Adaptability & Resilience: Manage change and conflict constructively

  • Communication & Relationship Building: Clear communication across global teams, strong stakeholder relationships


Work Environment & On-site Protocol

  • Roles may be site-essential, site-by-design, field-based, or remote-by-design

  • On-site presence is essential for collaboration and productivity in certain roles

  • Reasonable accommodations provided for employees with disabilities


Equal Opportunity & Compliance

  • BMS is an equal opportunity employer

  • Encourages applications even if requirements are not perfectly met

  • Recommends Covid-19 vaccination and boosters

  • Employment consideration for qualified applicants with arrest/conviction records per local laws

  • Data handled per applicable data privacy policies and regulations