Bristol Myers Squibb (BMS) is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines to help patients overcome serious diseases. With a strong focus on oncology, hematology, immunology, and cardiovascular diseases, BMS is at the forefront of medical advancements, transforming patient lives through cutting-edge research and patient-centric care.
At BMS, employees thrive in a challenging, meaningful, and life-changing work environment. The company fosters diversity, innovation, and career growth, offering competitive benefits, work-life balance, and opportunities to contribute to groundbreaking therapies.
1. Medical Science Liaison – Oncology & Hematology (Field Based, Mumbai)
Job Description
The Medical Science Liaison (MSL) serves as a scientific expert, engaging with healthcare professionals (HCPs) and thought leaders (TLs) to provide medical insights, support clinical discussions, and facilitate safe and appropriate use of BMS medicines.
Key Responsibilities:
- Develop and maintain relationships with oncology & hematology KOLs (Key Opinion Leaders).
- Provide scientific and clinical data on BMS products in a compliant manner.
- Support clinical trial activities, including site identification and investigator engagement.
- Contribute to medical strategies and patient advocacy programs.
- Ensure regulatory compliance and pharmacovigilance reporting.
Qualifications:
- MBBS, MD, BDS, MDS (Oncology/Hematology experience preferred).
- 1-2 years of Field Medical experience (Medical Affairs).
- Strong communication, presentation, and scientific engagement skills.
- Knowledge of clinical trials, HEOR (Health Economics & Outcomes Research), and regulatory guidelines.
📍 Location: Mumbai
2. ETMF Operations Analyst (Hyderabad)
Job Description
The eTMF (Electronic Trial Master File) Operations Analyst ensures the accuracy and completeness of clinical trial documentation, supporting inspection readiness and compliance with ICH/GCP guidelines.
Key Responsibilities:
- Upload and manage clinical trial documents in Veeva Vault eTMF.
- Perform Quality Validation (QV) checks on trial documents.
- Support User Acceptance Testing (UAT) for eTMF updates.
- Ensure ALCOA+ principles (data integrity) in document management.
- Collaborate with global clinical teams for compliance.
Qualifications:
- Bachelor’s degree in Life Sciences or related field.
- 3-5 years of eTMF experience (Veeva Vault preferred).
- Knowledge of clinical trial processes, regulatory submissions, and GCP.
- Strong project management and analytical skills.
📍 Location: Hyderabad
3. Clinical Trial Support Specialist (Hyderabad)
Job Description
The Clinical Trial Support Specialist ensures efficient document management, submissions, and regulatory compliance for clinical trials.
Key Responsibilities:
- Prepare submission-ready clinical documents (CSR appendices, financial disclosures).
- Maintain trial master files (eTMF/CTMS) and ensure data accuracy.
- Support drug shipment logistics (SAP integration).
- Ensure ICH/GCP compliance in trial documentation.
Qualifications:
- 2-4 years in clinical trial documentation management.
- Experience with Veeva Vault Clinical, CTMS, and MS Office.
- Knowledge of regulatory guidelines (FDA, ICH, GCP).
📍 Location: Hyderabad
How To Apply
🔗 Apply Here: BMS Careers – Clinical Trial Support Specialist
