Bristol Myers Squibb Hiring Global Trial Associate & Senior Global Trial Associate | Clinical Research Jobs 2026

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Bristol Myers Squibb Hiring Global Trial Associate & Senior Global Trial Associate | Clinical Research Jobs 2026

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Bristol Myers Squibb Hiring Global Trial Associate & Senior Global Trial Associate

🏢 Bristol Myers Squibb
📍 Hyderabad
🧪 Global Clinical Trials
📂 CTMS & eTMF
🎓 2–4 Years

Bristol Myers Squibb (BMS) is hiring Global Trial Associates and Senior Global Trial Associates in Hyderabad, India.

These opportunities are ideal for candidates interested in Clinical Trial Operations, Global Clinical Research, CTMS, eTMF, ICH-GCP Compliance, Vendor Management, and Clinical Project Coordination.

📋 Job Overview

  • Company: Bristol Myers Squibb (BMS)
  • Roles: Global Trial Associate / Senior Global Trial Associate
  • Location: Hyderabad, Telangana
  • Industry: Clinical Research / Pharma / Biotechnology
  • Job Type: Full-Time
  • Qualification: BA/BS in Life Sciences / Pharmacy / Clinical Research
  • Experience: 2–4 Years
  • Travel Requirement: Less than 5%
💰 Expected Salary: ₹7 – ₹14 LPA

🏢 About Bristol Myers Squibb

Bristol Myers Squibb is one of the world’s leading biopharmaceutical companies focused on innovative medicines and clinical research excellence.

The company offers global exposure, flexible work models, strong learning opportunities, and collaborative clinical development teams across multiple therapeutic areas.

🧪 Global Trial Associate Responsibilities

  • Support study startup, maintenance, and closeout activities
  • Manage study documentation and eTMF completeness
  • Assist with vendor invoice approvals and payment tracking
  • Maintain study SharePoint and vendor site lists
  • Participate in study meetings and documentation
  • Support CTMS updates and operational planning
  • Coordinate with internal and external stakeholders
  • Support study closure and archival activities
  • Ensure compliance with ICH-GCP and SOP requirements

🌍 Senior Global Trial Associate Responsibilities

  • Independently manage GTA operational activities
  • Support vendor oversight and payment tracking
  • Manage protocol milestones and CTMS planning
  • Contribute to process improvement initiatives
  • Mentor junior GTAs and team members
  • Support regulatory and ethics committee approvals
  • Track non-clinical supplies and study deliverables
  • Collaborate with global cross-functional teams

🎓 Eligibility Criteria

Eligible Qualifications

  • B.Pharm / M.Pharm / Pharm.D
  • BSc / MSc Life Sciences
  • Clinical Research
  • Biotechnology & Related Disciplines

🧑‍💻 Experience Required

  • 2–4 Years in Clinical Research
  • Experience with CTMS and eTMF systems preferred

⭐ Preferred Skills

  • ICH-GCP guidelines knowledge
  • Clinical trial operations understanding
  • Vendor and payment tracking experience
  • Project coordination abilities
  • Risk management and stakeholder communication
  • Strong presentation and teamwork skills

🌍 Why Join Bristol Myers Squibb?

  • Global clinical research exposure
  • Hybrid and flexible work opportunities
  • Career growth and internal mobility
  • Inclusive and collaborative work culture
  • Competitive compensation and employee benefits
  • Opportunity to work on innovative therapies

📄 Resume & Interview Tips

  • Highlight CTMS and eTMF experience
  • Mention global trial coordination exposure
  • Add ICH-GCP and SOP compliance knowledge
  • Showcase vendor management and documentation skills
  • Keep resume ATS-friendly and concise

🚀 Job Application Links

📌 Important Note Before You Apply:

Please make sure to read the complete job description carefully before submitting your application. Make sure your Clinical Trial Operations, CTMS, and eTMF experience aligns with the selected role requirements before proceeding.
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