Looking for Senior Specialist Patient Safety jobs in Hyderabad? Bristol Myers Squibb (BMS) is hiring a Senior Specialist, International Patient Safety to join its Global Pharmacovigilance team in Hyderabad, Telangana.
This is an excellent opportunity for professionals with 1โ2 years of pharmacovigilance (PV), drug safety, ICSR processing, risk management, aggregate reporting, or medical information experience to work with one of the world’s leading biopharmaceutical companies. Candidates with Life Sciences or Nursing backgrounds who want to advance their careers in International Patient Safety, Pharmacovigilance, Drug Safety, and Regulatory Compliance are encouraged to apply.
Job Details
| Details | Information |
|---|---|
| Job Title | Senior Specialist, International Patient Safety |
| Company | Bristol Myers Squibb (BMS) |
| Location | Hyderabad, Telangana, India |
| Department | International Patient Safety |
| Job Type | Full-Time |
| Experience | 1โ2 Years |
| Qualification | Life Sciences Degree or Nursing Qualification |
| Job Requisition ID | R1600822 |
| Posted Date | June 30, 2026 |
Key Responsibilities
The selected candidate will support global pharmacovigilance operations and ensure compliance with international safety regulations.
Responsibilities include:
- Create and maintain Risk Management Plans (RMPs)
- Support implementation of Additional Risk Minimisation Measures
- Manage Pharmacovigilance safety mailboxes and communications
- Support Aggregate Safety Reports
- Maintain PV awareness and training materials
- Implement Pharmacovigilance Agreements (PVAs)
- Process Individual Case Safety Reports (ICSRs)
- Perform literature screening for adverse events
- Submit safety reports to Health Authorities and Ethics Committees
- Maintain PV System Master File (PSMF)
- Manage deviations, CAPA, and quality activities
- Prepare PV documentation for distributors and local representatives
- Monitor third-party PV performance against KPIs
- Coordinate signal communications with regulatory authorities
- Support Pharmacovigilance audits and inspections
- Collaborate with cross-functional global safety teams
Required Qualifications
Applicants should possess:
- Bachelor’s or Master’s degree in Life Sciences
- Nursing qualification is also acceptable
- 1โ2 years of experience in:
- Pharmacovigilance
- Drug Safety
- Medical Information
- Pharmaceutical Industry
- Knowledge of:
- ICH Guidelines
- CIOMS
- Pharmacovigilance Regulations
- Risk Management Plans
- ICSR Processing
- Aggregate Reports
- Excellent written and spoken English
- Strong communication and organizational skills
- Ability to manage multiple deadlines
- Basic digital tools and process automation knowledge
- Analytical and problem-solving abilities
Preferred Skills
Successful candidates should have experience with:
- Pharmacovigilance Agreements
- Literature Screening
- Signal Management
- Safety Data Quality
- CAPA Management
- PSMF Maintenance
- Regulatory Submissions
- Ethics Committee Reporting
- Distributor Oversight
- Quality Compliance
Why Join Bristol Myers Squibb?
Bristol Myers Squibb offers employees an opportunity to work on life-changing medicines while building a rewarding global career.
Benefits include:
- Global Pharmacovigilance exposure
- Career growth opportunities
- Competitive compensation
- Flexible work culture
- Learning and development programs
- Inclusive workplace
- International collaboration
- Comprehensive employee benefits
Who Should Apply?
This role is ideal for professionals working as:
- Pharmacovigilance Associate
- Drug Safety Associate
- Patient Safety Specialist
- ICSR Specialist
- Medical Information Associate
- PV Compliance Executive
- Safety Operations Associate
- Risk Management Associate
How to Apply
