If you’re looking for Pharmacovigilance jobs in Bangalore or want to build a career in Drug Safety, Fortrea is hiring for the position of Safety Science Coordinator II in Bangalore, India. This opportunity is ideal for candidates with a background in Pharmacy, Life Sciences, Nursing, Medical Sciences, or Biological Sciences who have relevant pharmacovigilance or clinical safety experience.
As a Safety Science Coordinator II, you will support adverse event processing, regulatory safety reporting, safety database management, and pharmacovigilance compliance while working with global clinical research teams. Candidates interested in Drug Safety Associate jobs, Pharmacovigilance Coordinator jobs, or Clinical Safety jobs in India should consider applying before July 14, 2026.
Job Overview
| Job Details | Information |
|---|---|
| Company | Fortrea |
| Position | Safety Science Coordinator II |
| Location | Bangalore, Karnataka, India |
| Job Type | Full-Time |
| Department | Pharmacovigilance / Clinical Safety |
| Application Deadline | July 14, 2026 |
| Experience | 1+ Year Relevant Experience |
| Education | B.Pharm, M.Pharm, PharmD, B.Sc, M.Sc, Nursing, Medical Sciences, Life Sciences |
Key Responsibilities
The selected candidate will:
- Process adverse event reports received from clinical trials and post-marketing sources.
- Perform accurate safety data entry into pharmacovigilance databases.
- Review Individual Case Safety Reports (ICSRs) for completeness and accuracy.
- Prepare patient narratives for adverse event cases.
- Code adverse events using MedDRA.
- Generate follow-up queries for missing clinical information.
- Ensure timely expedited reporting to regulatory authorities and sponsors.
- Submit Serious Adverse Event (SAE) reports within regulatory timelines.
- Support Periodic Safety Reports (PSRs) and Expedited Safety Reports (ESRs).
- Maintain project documentation and pharmacovigilance tracking systems.
- Participate in database reconciliation activities.
- Conduct quality review and peer review of safety cases.
- Support audits, inspections, and quality management activities.
- Follow SOPs, work instructions, GVP guidelines, and regulatory requirements.
- Assist in client meetings and project discussions.
- Mentor junior team members whenever required.
Required Qualifications
Candidates should possess any of the following:
- B.Pharm
- M.Pharm
- PharmD
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biological Sciences
- Nursing
- Medical Sciences
- Related healthcare or life science degree
Minimum Experience:
- Bachelor’s Degree + 1 year relevant experience
- Associate Degree + 1 year Safety experience
- Non-degree candidates with 3 years relevant experience
- PharmD candidates with 1 year experience or residency/fellowship
Preferred Skills
Applicants should demonstrate:
- Knowledge of Pharmacovigilance processes
- Understanding of Adverse Event Reporting
- MedDRA coding knowledge
- Strong attention to detail
- Good written and verbal communication
- MS Office proficiency
- Ability to work independently
- Team collaboration skills
- Quality-focused approach
- Time management skills
Why Join Fortrea?
Working at Fortrea provides exposure to global clinical research programs and pharmacovigilance operations. Employees gain valuable experience in:
- Global Drug Safety Operations
- Clinical Trial Safety Management
- Regulatory Compliance
- Pharmacovigilance Reporting
- International Client Interaction
- Career Growth in Clinical Research
- Continuous Learning & Development
- Collaborative Global Teams
Who Should Apply?
This role is ideal for:
- B.Pharm Freshers with relevant internship experience
- Experienced Pharmacovigilance Associates
- Drug Safety Associates
- Clinical Safety Professionals
- PharmD Graduates
- Life Science Graduates
- Nursing Professionals
- Medical Science Graduates
How to Apply
