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Associate Global Trial Manager

10 years
Not Disclosed
10 Nov. 20, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 Global Trial Manager – Hyderabad, India

Category: Clinical Research
Experience Required: Minimum 10 years in clinical research or global study operations

Job Overview

Bristol Myers Squibb (BMS) is hiring an Associate Global Trial Manager to support global clinical study operations and delivery. This position plays a key role in overseeing study execution, ensuring operational excellence, managing study documentation, and strengthening collaboration across global teams.

This role is ideal for experienced clinical research professionals who bring strong project management capabilities, deep knowledge of ICH/GCP guidelines, and the ability to support high-quality global clinical trial delivery.


Key Responsibilities

Project Management & Study Oversight

  • Support and coordinate global study execution using performance metrics and quality indicators.

  • Manage or oversee clinical monitoring quality and ensure adherence to study plans and standard processes.

  • Track and manage study deliverables such as timelines, CTMS updates, documentation, and communication plans.

  • Identify potential study risks and support the Global Trial Lead (GTL) in developing mitigation strategies.

  • Escalate operational issues and provide timely updates to GTL and leadership teams.

  • Contribute to data-driven decision-making across assigned studies.

Study Planning, Conduct, and Closure

  • Support the development, collection, and maintenance of study-level documentation and ensure eTMF completeness and accuracy.

  • Assist GTL in reviewing key documents such as study protocols, ICFs, CRFs, data review plans, edit specifications, and CSR components.

  • Support country and site feasibility assessments using relevant clinical and operational data.

  • Assist with study recruitment and retention initiatives where required.

  • Oversee study-specific CSR appendices and documentation as assigned.

  • Coordinate responses to regulatory, IRB/IEC, and country-specific submissions.

  • Review protocol deviations, study trackers, and act as part of audit response and CAPA processes.

  • Manage assigned study types (e.g., NPP, HEOR) from start-up through close-out if applicable.

  • Manage vendor invoices, budget worksheets, forecasting, and accruals with GTL oversight.

Collaboration & Leadership

  • Act as a mentor to junior Global Trial Associates.

  • Support cross-functional collaboration across therapeutic areas and global study teams.

  • Contribute to meeting preparation, agenda development, and documentation for assigned studies.

  • Maintain composure and professionalism during periods of high operational demand.

  • Engage in strategy discussions and contribute to continuous improvement initiatives.


Required Qualifications and Experience

  • Education: BA/BS degree or equivalent in a life science or related field.

  • Experience:

    • Minimum 10 years of clinical research or global study operations experience.

    • Understanding of global regulatory environments and submission timelines.

    • Experience working with Clinical Trial Management Systems (CTMS) and Clinical Trial Master File (TMF) platforms.

  • Technical Skills:

    • Strong understanding of ICH/GCP guidelines, clinical research processes, and regulatory frameworks.

    • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).

  • Competencies:

    • Project management experience within the clinical or healthcare industry.

    • Ability to handle multiple priorities and shifting timelines.

    • Strong interpersonal, communication, and cross-functional collaboration skills.

    • Ability to provide insights, support decision-making, and manage study-level activities independently.

  • Travel: Up to 5% as required.


Why Join Bristol Myers Squibb

At BMS, every employee contributes to the mission of transforming patients’ lives through science. You will work in a diverse, collaborative, and innovative environment with opportunities for global exposure, professional development, and meaningful impact.


Work Model

BMS follows a structured workplace model:

  • Site-Essential: Full onsite presence required.

  • Site-by-Design: Hybrid (minimum 50% onsite).

  • Field-Based/Remote-by-Design: Travel as required for business needs.

This role follows the applicable occupancy guidelines based on assigned responsibilities.