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Bristol Myers Squibb Hiring Clinical Trial Support Specialist | Clinical Research Opportunity
🏢 Bristol Myers Squibb (BMS)
📍 Hyderabad
📄 Clinical Trial Support Specialist
🏠 Hybrid Eligible
Bristol Myers Squibb (BMS) is hiring Clinical Trial Support Specialists for its Hyderabad office. This opportunity is ideal for candidates interested in Clinical Operations, TMF Management, CTMS Administration, Regulatory Documentation, and Clinical Trial Support activities.
The role provides exposure to global drug development programs, clinical documentation management, inspection readiness, submission support, and cross-functional clinical research operations.
📋 Job Overview
| Details | Information |
|---|---|
| Position | Clinical Trial Support Specialist |
| Company | Bristol Myers Squibb (BMS) |
| Location | Hyderabad, Telangana |
| Job Type | Full-Time |
| Department | Clinical Operations / Clinical Trial Support |
| Work Model | Site-by-Design (Hybrid) |
| Requisition ID | R1602784 |
| Industry | Clinical Research |
💰 Expected Salary Range: ₹5 LPA – ₹10 LPA
🏢 About Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. The company is widely recognized for its contributions to oncology, immunology, cardiovascular, and other therapeutic areas.
📌 Key Responsibilities
- Prepare clinical trial submission documents according to regulatory requirements.
- Support submission managers in developing submission-ready documentation.
- Manage Clinical Study Report (CSR) appendices and financial disclosure documentation.
- Maintain Submission Ready Compliance (SRC) standards.
- Coordinate clinical trial site number creation and maintenance.
- Maintain site milestones and regulatory approval information.
- Manage investigational product shipment addresses and SAP data.
- Perform reconciliation activities between Veeva eTMF and CTMS systems.
- Support trial master file quality and inspection readiness.
- Identify operational risks and implement mitigation strategies.
- Ensure ICH-GCP and SOP compliance.
- Collaborate with global clinical development teams.
📚 Clinical Research Resources
👉 Clinical Research Coordinator Career Guide
👉 CRA Knowledge Quiz
👉 Clinical Trial Assistant Quiz
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc
- M.Sc
- Life Sciences
- Biotechnology
- Clinical Research
- Healthcare
- Related Scientific Disciplines
Preferred Qualifications:
- Understanding of Clinical Trial Processes
- Knowledge of ICH-GCP Guidelines
- TMF & Clinical Documentation Knowledge
- Veeva Systems Familiarity Preferred
- Project Management Skills
💡 Essential Skills
- Clinical Operations Support
- Clinical Trial Documentation Management
- TMF & eTMF Management
- CTMS Administration
- Regulatory Submission Support
- Veeva Systems Knowledge
- Clinical Study Report Documentation
- Trial Master File Reconciliation
- ICH-GCP Compliance
- Quality & Inspection Readiness
- Clinical Research Coordination
- SAP Data Management
- Project Management
- Cross-functional Collaboration
- Regulatory Affairs Support
🎁 Why Join Bristol Myers Squibb?
- Exposure to global clinical development programs.
- Opportunity to work with leading oncology research teams.
- Career growth within Clinical Operations and Drug Development.
- Competitive compensation and employee benefits.
- Flexible and collaborative work culture.
- Learning and development opportunities.
- Diverse and inclusive workplace environment.
📈 Career Growth Opportunities
This Clinical Trial Support Specialist role can lead to several advanced Clinical Research and Clinical Operations positions, including:
- Clinical Trial Associate (CTA)
- Clinical Operations Specialist
- TMF Specialist
- Clinical Project Coordinator
- Study Start-Up Specialist
- Clinical Trial Manager
- Clinical Project Manager
- Regulatory Operations Specialist
📄 Resume & Interview Preparation Tips
- Highlight Clinical Research, TMF, CTMS, and Documentation experience.
- Mention knowledge of ICH-GCP guidelines and Clinical Trial processes.
- Showcase organizational and project coordination skills.
- Add experience with Veeva, eTMF, CTMS, or Clinical Systems if applicable.
- Keep your resume ATS-friendly and professionally formatted.
🧠 Practice & Learning Resources
👉 Clinical Trial Assistant Quiz
👉 CRA Knowledge Quiz
👉 Explore Healthcare Quizzes
📝 How to Apply
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Highlight Clinical Research, Documentation, TMF, and Regulatory experience.
- Complete the 15-second countdown timer to unlock the application button.
- Apply only if your profile matches the role requirements.
🚀 Apply for Clinical Trial Support Specialist
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📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements. Applying thoughtfully increases your chances of being shortlisted and creates a strong professional impression.
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements. Applying thoughtfully increases your chances of being shortlisted and creates a strong professional impression.
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