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
