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