Bristol Myers Squibb (BMS), a global leader in biopharmaceutical innovation, has announced three new openings in Clinical Trial Transparency and Submission Operations. These roles support the company’s commitment to regulatory compliance, public disclosure, and patient-focused drug development.
These full-time positions are based in Hyderabad, Telangana, India, offering opportunities to work with cross-functional scientific, medical, and regulatory experts.
🧪 Open Positions at BMS Hyderabad
1️⃣ Clinical Trial Registration Sr. Specialist
Key Responsibilities:
- Manage clinical trial registrations on ClinicalTrials.gov, EU PAS, and global registries
- Coordinate with clinical, regulatory, and safety teams
- Ensure timely updates to public records and compliance with NIH and global guidelines
- Maintain study trackers and educate teams on registry compliance
Qualifications:
- Bachelor’s degree in Science
- Minimum 3 years of pharma/CRO experience
- Knowledge of regulatory compliance, transparency, and CT operations preferred
2️⃣ Clinical Trial Disclosure Manager
Key Responsibilities:
- Oversee redaction compliance under EMA Policy 0070, PRCI, EU CTR
- Ensure operational execution of disclosure deliverables
- Manage vendors, stakeholder communication, SOP improvements
- Support regulatory updates and cross-functional change management
Qualifications:
- Bachelor’s/Master’s in a scientific or medical domain
- 6–8 years of experience with 3–4 years in transparency
- Strong understanding of global clinical trial disclosure policies
3️⃣ Clinical Trial Submission Document Specialist
Key Responsibilities:
- Support FDA submission deliverables, including CSR appendices
- Perform formatting checks and submission readiness compliance
- Work with CTSS and cross-functional teams
- Use platforms like Veeva Vault, CTMS, SharePoint, TMF systems
Qualifications:
- Bachelor’s in Life Sciences/Business
- 1–4 years of clinical documentation or pharma environment experience
- Knowledge of ICH-GCP, document management, regulatory submission workflows
🎯 Key Skills Required Across Roles
✔ Clinical trial operations
✔ Regulatory compliance (FDA, EMA, EU CTR, NIH)
✔ Veeva Vault / CTMS / TMF knowledge (preferred)
✔ Project management & stakeholder communication
✔ Strong documentation, analytical, and organizational abilities
💼 Why Work at Bristol Myers Squibb?
- 💡 Meaningful, patient-impacting work
- 🌍 Global exposure across multiple therapeutic areas
- 🧭 Hybrid flexibility for eligible roles
- 🎓 Learning and cross-functional growth opportunities
📍 Job Location
📍 Hyderabad, Telangana, India
📝 How to Apply
Application Link for Clinical Trial Registration Sr. Specialist
Application Link for CT Disclosure Manager
Application Link for CT Submission Specialist
