Bristol Myers Squibb Hiring Senior Global Trial Associate | Hyderabad
Bristol Myers Squibb (BMS) is hiring a Senior Global Trial Associate in Hyderabad, India. This exciting opportunity is ideal for professionals with experience in Clinical Research, Clinical Operations, CTMS, eTMF Management, and Global Trial Operations.
The selected candidate will work closely with global study teams and contribute to the execution of innovative clinical trials that support the development of life-changing therapies.
📋 Job Overview
| Details | Information |
|---|---|
| Position | Senior Global Trial Associate |
| Company | Bristol Myers Squibb (BMS) |
| Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Experience | 2–4 Years |
| Industry | Clinical Research / Pharmaceutical / Biotechnology |
| Requisition ID | R1600982 |
| Work Model | Hybrid / Site-Based |
🏢 About Bristol Myers Squibb
Bristol Myers Squibb is one of the world's leading biopharmaceutical companies focused on discovering, developing, and delivering innovative medicines for patients with serious diseases.
The company provides employees with opportunities to work on global clinical trials, collaborate with international teams, and contribute to the development of life-changing therapies.
📌 Key Responsibilities
🧪 Clinical Trial Management
- Support Global Trial Leads (GTLs) in managing global clinical studies.
- Maintain study timelines, plans, and study documentation.
- Ensure eTMF completeness and inspection readiness.
- Update protocol milestones and country planning information in CTMS.
- Support study startup, maintenance, and closeout activities.
📊 Project Coordination
- Facilitate study team meetings.
- Prepare and maintain meeting minutes.
- Monitor study performance metrics.
- Identify operational risks and support mitigation strategies.
- Coordinate activities across global cross-functional teams.
💰 Vendor & Budget Management
- Support vendor oversight activities.
- Review vendor invoices and payment processing.
- Track study accruals and budgets.
- Manage Statements of Work (SOWs) and vendor contracts.
📑 Regulatory & Compliance Support
- Support country-specific regulatory submissions.
- Assist with IRB/IEC notifications and approvals.
- Ensure compliance with SOPs and ICH-GCP guidelines.
📦 Study Closure Activities
- Lead assigned archival and study closure activities.
- Support Clinical Study Report (CSR) appendices.
- Ensure proper documentation during trial closeout.
🎓 Required Qualifications
- Life Sciences
- Pharmacy
- Biotechnology
- Nursing
- Clinical Research
- Related Healthcare Discipline
Experience Required: 2–4 Years in Clinical Research or Clinical Operations.
⭐ Technical Skills
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF)
- ICH-GCP Guidelines
- Clinical Trial Documentation
- Vendor Management
- Budget Tracking
- Regulatory Compliance
- Clinical Study Operations
🎁 Benefits at BMS
- Global Clinical Trial Exposure
- Career Growth Opportunities
- Competitive Compensation Package
- Learning & Development Programs
- Collaborative Work Culture
- Flexible Working Arrangements
- Work on Life-Changing Therapies
🚀 Career Scope
Working as a Senior Global Trial Associate provides strong exposure to Global Clinical Operations, Trial Management, Regulatory Compliance, Vendor Management, and Clinical Project Coordination.
Future career paths may include Global Trial Lead, Clinical Trial Manager, Clinical Operations Manager, Study Manager, Project Manager, and Clinical Program Manager roles.
📄 ATS-Friendly Resume Tips
- Add keywords such as CTMS, eTMF, Clinical Operations, Global Trials, ICH-GCP, Vendor Management, Study Startup, and Trial Closeout.
- Highlight experience in study coordination and clinical documentation.
- Mention global trial exposure and stakeholder management.
- Quantify achievements wherever possible.
- Use a clean ATS-friendly resume format.
💡 Interview Preparation Tips
- Review CTMS and eTMF concepts.
- Understand ICH-GCP requirements.
- Prepare examples of study coordination activities.
- Be ready to discuss risk management and vendor oversight.
- Review global clinical trial lifecycle processes.
📝 How to Apply
- Review the complete job description.
- Prepare an updated ATS-friendly resume.
- Complete the countdown timer below.
- Apply through the official BMS Careers portal.
🚀 Job Application Link
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
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