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Ad Global Trial Lead

Bristol Myers Squibb
Bristol Myers Squibb
2+ years
Not Disclosed
Hyderabad
10 May 6, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Associate Director (AD), Global Trial Lead


Company

Bristol Myers Squibb (BMS)

Bristol Myers Squibb


Location

Hyderabad, Telangana, India (Hybrid / Site-essential or site-by-design depending on assignment)


Job Type

Full-time


Job Requisition ID

R1598473


Job Summary

This is a senior clinical operations leadership role responsible for end-to-end global clinical trial oversight, including:

  • Study planning and execution

  • Vendor and CRO management

  • Budget and financial oversight

  • Cross-functional study leadership

  • Risk management and operational strategy

The role ensures timely, cost-effective, and high-quality clinical trial delivery across the study lifecycle.


Key Responsibilities

1. Clinical Trial Project Management

  • Lead global and cross-functional clinical trial execution

  • Ensure delivery against:

    • Timelines

    • Budget

    • Quality standards

  • Coordinate internal teams and external vendors (CROs, AROs)


2. Vendor & CRO Management

  • Manage Scope of Work (SOW) for CROs and vendors

  • Participate in vendor selection and evaluation

  • Review and approve:

    • Vendor invoices

    • Budget accruals

    • Scope changes

  • Ensure vendor performance aligns with contract and quality expectations


3. Study Strategy & Operational Oversight

  • Provide strategic input on study feasibility and protocol execution

  • Guide operational planning from study start-up to close-out

  • Identify and manage risks across trials

  • Develop mitigation and contingency plans


4. Financial & Budget Management

  • Lead study-level budget planning with cross-functional teams

  • Conduct quarterly budget reviews and forecasting

  • Monitor variances and coordinate with Finance

  • Resolve cost and timeline deviations


5. Trial Systems & Documentation

  • Maintain study records in systems such as:

    • CTMS

    • eTMF (Veeva Vault)

  • Ensure data accuracy and audit readiness

  • Maintain project management tools:

    • Risk logs

    • Issue trackers

    • Decision logs

    • Action trackers


6. Cross-functional Leadership

  • Lead global study teams across functions

  • Coordinate with:

    • Clinical Research

    • Development teams

    • Affiliates

    • External partners

  • Ensure information sharing and alignment across stakeholders


7. Risk Management & Issue Resolution

  • Identify operational risks early

  • Balance trade-offs between:

    • Cost

    • Quality

    • Timelines

  • Implement corrective actions and mitigation strategies


8. Mentorship & Team Development

  • Mentor Global Development Operations (GDO) team members

  • Support capability development and training

  • Promote best practices across teams


Required Qualifications

Education

  • Bachelor’s degree (required)

  • Advanced degree preferred (Life Sciences or related field)


Experience

  • Strong experience in clinical trial management / clinical operations

  • Background in:

    • Global clinical studies

    • CRO/vendor management

    • Budget oversight

  • Experience leading cross-functional teams


Core Skills

  • Strong project management capability

  • Vendor negotiation and oversight skills

  • Financial planning and forecasting experience

  • Risk management in clinical trials

  • Strong stakeholder management skills


Technical Knowledge

  • Clinical trial systems:

    • CTMS

    • eTMF (preferred: Veeva Vault)

  • Understanding of clinical development lifecycle


Leadership Skills

  • Cross-functional leadership in matrix organizations

  • Ability to influence without direct authority

  • Strong communication and decision-making ability

  • Ability to manage global teams and complex programs


Role Characteristics

  • Senior leadership (Associate Director level)

  • Highly strategic + operational hybrid role

  • Strong focus on execution governance and financial control

  • Heavy cross-functional and vendor-facing responsibility


Key Impact Areas

  • Global clinical trial success and delivery

  • Budget efficiency and cost control

  • Vendor performance optimization

  • Risk reduction in clinical execution

  • Portfolio-level operational consistency


Work Model

  • Hybrid (site presence required depending on role classification)


How This Role Differs

Compared to other roles you shared:

  • Higher level than CRA / Data / System Lead roles

  • More program ownership + leadership + budget control

  • Less hands-on systems work, more decision-making and oversight