Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative medicines for patients with serious diseases. With a strong focus on oncology, hematology, immunology, and cardiovascular diseases, BMS is at the forefront of transforming patients’ lives through cutting-edge science.
Currently, BMS is hiring for three key roles in Hyderabad, India, offering professionals an opportunity to contribute to groundbreaking clinical trials. Below are the details for each position:
1. Clinical Trial Support Specialists, Line Lead
Job ID: R1589412
Location: Hyderabad (Hybrid)
Experience: 5-7 years
Job Description:
- Lead a team responsible for reconciling and preparing clinical trial submission documents in compliance with regulatory guidelines.
- Oversee Clinical Trial Management System (CTMS) activities, ensuring adherence to ICH/GCP guidelines.
- Collaborate with cross-functional teams and CROs to streamline regulatory submissions.
- Drive process improvements and maintain compliance with global regulatory requirements.
- Strong expertise in Veeva Vault Clinical and document management systems.
Qualifications:
- Bachelor’s degree in Life Sciences or related field (advanced degree preferred).
- 5-7 years of experience in clinical operations, regulatory submissions, or trial management.
- Strong leadership, project management, and analytical skills.
2. Document Coordinator, Global Trial Acceleration
Job ID: R1584568
Location: Hyderabad (Full-time)
Experience: 3+ years
Job Description:
- Manage clinical trial document collection, review, and approval across global trials.
- Support study start-up, regulatory submissions, and site activation processes.
- Coordinate with CROs, investigators, and internal teams to ensure compliance.
- Review Site Monitoring Visit reports and track issue resolution.
- Experience with Veeva Vault, CTMS, and eTMF systems preferred.
Qualifications:
- Bachelor’s degree in Life Sciences, Business Administration, or related field.
- 3+ years in clinical operations, regulatory documentation, or CRO management.
- Strong knowledge of ICH/GCP guidelines and clinical trial processes.
3. Clinical Trial Support Specialist
Job ID: R1590578
Location: Hyderabad (Hybrid)
Experience: 2-4 years
Job Description:
- Assist in preparing submission-ready clinical trial documents (CSR appendices, financial disclosures).
- Maintain Veeva Vault CTMS/eTMF for accurate trial data tracking.
- Ensure compliance with BMS SOPs and regulatory guidelines.
- Support drug shipment logistics and site activation processes.
Qualifications:
- 2-4 years in clinical trial documentation or regulatory support.
- Experience with Veeva Vault Clinical, SharePoint, and MS Office.
- Strong understanding of GCP, ICH guidelines, and clinical trial operations.
Why Join Bristol Myers Squibb?
- Impactful Work: Contribute to life-changing therapies for patients worldwide.
- Career Growth: Opportunities for professional development in a global biopharma leader.
- Inclusive Culture: A diverse and collaborative work environment.
- Flexible Work Model: Hybrid and on-site options based on role requirements.
How to Apply?
Application Link For Clinical Trial Support Specialists, Line Lead
Application Link For Document Coordinator, Global Trial Acceleration
Application Link For Clinical Trial Support Specialist
