Bristol Myers Squibb (BMS), a global biopharma leader transforming patients’ lives through science, has announced multiple job openings across India. These include roles in Clinical Trial Operations, Regulatory Documentation, Supply Chain, and Sales Management.
If you’re passionate about advancing clinical research and patient care, these new openings at BMS Hyderabad and Delhi could be your gateway to a life-changing career in pharmaceuticals.
🔹 1. Clinical Trial Registration Sr. Specialist – Hyderabad
Division: Research & Development
Function: Global Development Operations / Trial Delivery Support (TDS)
Location: Hyderabad, Telangana
Responsibilities
- Register and maintain clinical trials on public databases (ClinicalTrials.gov, EU PAS).
- Liaise with global trial teams to ensure accuracy and regulatory compliance.
- Manage updates, documentation, and trackers to maintain transparency.
- Support education of teams on NIH and registry requirements.
Qualifications
- Bachelor’s in Life Sciences or related field.
- Minimum 3 years’ experience in clinical research, regulatory, or transparency roles.
- Strong communication, organization, and analytical skills.
🔹 2. CT Submission Specialist – Hyderabad
Job Title: GDO Submission Document Specialist
Division: Global Development Operations
Responsibilities
- Prepare, quality-check, and manage clinical submission deliverables.
- Collaborate with teams for CSR appendices, financial disclosures, and documentation.
- Ensure submissions meet global compliance and formatting standards.
- Support document management using systems like Veeva Vault and CTMS.
Qualifications
- Bachelor’s degree in Life Sciences or Business.
- 3–4 years of pharma/biotech experience, with 1–2 years in clinical documentation.
- Strong knowledge of ICH-GCP, clinical trial master file systems, and regulatory processes.
🔹 3. Clinical Supply Chain Associate – Hyderabad
Position Type: Full-time | Early Career
Department: Clinical Supply Chain Operations
Responsibilities
- Assist in clinical study supply planning and inventory control.
- Forecast supplies based on patient enrollment and dosing schedules.
- Coordinate with depots and logistics teams for on-time delivery.
- Support customs clearance, documentation, and audit readiness.
Qualifications
- Bachelor’s degree in Science, IT, or Business (Supply Chain focus preferred).
- Internship or project experience in pharma supply chain is a plus.
- Strong analytical, communication, and Excel skills.
🔹 4. Manager – Clinical Trial Risk Analyst – Hyderabad
Department: Trial Delivery Support (TDS) / TRIM
Responsibilities
- Conduct data-driven risk analysis across global clinical trials.
- Collaborate with study teams to identify quality and compliance risks.
- Develop and monitor Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs).
- Support governance reporting, audits, and CAPA processes.
Qualifications
- Bachelor’s in Life Sciences, Data Science, or Analytics.
- 3+ years in clinical operations with expertise in Risk-Based Monitoring (RBM).
- Proficient in data visualization and analytical storytelling.
🔹 5. Specialty Care Advisor – Delhi (Field Based)
Division: Specialty Care Sales
Territory: Delhi NCR & Northern India
Responsibilities
- Drive product sales and awareness within assigned territories.
- Engage with doctors, pharmacists, and hospital authorities.
- Manage formulary inclusion and organize scientific meetings.
- Ensure compliance with ethical marketing and BMS values.
Qualifications
- Graduate in Pharmacy or Science; MBA preferred.
- Minimum 5 years of pharma sales experience (Oncology preferred).
- Excellent communication and relationship management skills.
| No. | Job Title | Location | Experience Required | Educational Qualification | Preferred Background |
|---|---|---|---|---|---|
| 1 | Clinical Trial Registration Sr. Specialist | Hyderabad | 3–5 years in clinical research, regulatory operations, or transparency roles | Bachelor’s or Master’s in Life Sciences, Pharmacy, Biotechnology, or related field | Experience with ClinicalTrials.gov, EudraCT, or public registry submissions preferred |
| 2 | CT Submission Specialist (GDO Submission Document Specialist) | Hyderabad | 3–4 years in pharma/biotech with 1–2 years in clinical documentation/submission support | Bachelor’s in Life Sciences, Pharmacy, Biotechnology, or Business Administration | Experience with Veeva Vault, TMF, CSR, CTD documentation |
| 3 | Clinical Supply Chain Associate | Hyderabad | 0–2 years (fresh graduates or early career professionals welcome) | Bachelor’s in Science, Pharmacy, Supply Chain Management, or Business | Internship or project in pharma supply planning/logistics advantageous |
| 4 | Manager – Clinical Trial Risk Analyst (TRIM) | Hyderabad | 3–6 years in clinical operations, risk management, or data analytics | Bachelor’s or Master’s in Life Sciences, Data Science, Statistics, or Pharmacy | Experience with Risk-Based Monitoring (RBM) and Quality Tolerance Limits (QTL) preferred |
| 5 | Specialty Care Advisor (Sales) | Delhi NCR | 5+ years in pharmaceutical sales (Oncology or Specialty segment) | Graduate in Pharmacy or Life Sciences; MBA preferred | Experience in hospital & specialty product marketing |
đź’Ľ Why Join Bristol Myers Squibb?
- Global impact: Contribute to groundbreaking research improving patient lives.
- Career growth: Continuous learning and structured development paths.
- Inclusive culture: BMS promotes flexibility, diversity, and hybrid work options.
- Employee well-being: Competitive benefits and wellness initiatives.
đź“ť How to Apply
Application Link Clinical Trial Registration Sr. Specialist – R1596332
Application Link CT Submission Specialist – R1596335
Application Link Clinical Supply Chain Associate – R1596660
Application Link Manager, Clinical Trial Risk Analyst – R1596340
Application Link Specialty Care Advisor – R1596838
