Fortrea Hiring Safety Science Coordinator II | Bangalore | Pharmacovigilance Jobs
Are you seeking Fortrea Careers Bangalore or a Pharmacovigilance Job in Bangalore? Global clinical research organization (CRO) Fortrea has announced recruitment for the position of Safety Science Coordinator II at its Bangalore office.
This clinical safety coordinator vacancy is ideal for pharmacy, life science, nursing, and medical graduates with at least one year of experience processing adverse events, managing safety databases, or coding in MedDRA. To draft a resume reflecting pharmacovigilance case-processing milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Fortrea (Fortrea Development India Private Limited) |
| Position | Safety Science Coordinator II |
| Job Location | Bangalore, Karnataka, India |
| Department | Pharmacovigilance & Clinical Safety (PSS) |
| Employment Type | Full-Time |
| Experience Required | 1+ Year of Clinical Safety / PV Experience |
| Qualifications | B.Pharm, M.Pharm, PharmD, B.Sc, M.Sc Life Sciences, Nursing, Medical Sciences |
| Application Deadline | July 14, 2026 |
💼 Key Responsibilities
- Adverse Event Processing: Process and manage adverse event reports from clinical trials and post-marketing settings.
- ICSR Data Entry: Perform data entry of clinical safety profiles into adverse event databases and tracking systems.
- Quality Review: Review Individual Case Safety Reports (ICSRs) for completeness, accuracy, and appropriateness for expedited reporting.
- Technical Narrative Writing: Write detailed patient narratives and code adverse events accurately using MedDRA terminology.
- Query Generation: Identify missing clinical information in initial reports and generate queries to site coordinators for collection.
- Expedited Reporting: Prioritize and submit expedited Serious Adverse Event (SAE) reports to sponsors, regulatory authorities, and ethics committees within strict regulatory timelines.
- Report Management: Perform processing and submission tasks for Periodic Safety Reports (PSRs) and Expedited Safety Reports (ESRs).
- Reconciliation & Compliance: Support database reconciliation, maintain study documentation, and ensure compliance with SOPs, GVP guidelines, and safety metrics.
To learn how safety science coordinator salaries compare to drug safety associate and clinical data manager structures in major CROs, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
- Education: Degree preferred in one or more of the following: Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related fields.
- Experience Matrix:
- Bachelor's/Master's Degree + 1 year of relevant safety/clinical trial experience.
- Associate Degree + 1 year of safety experience (or 2 years relevant experience).
- Non-degree candidates with 3 years of relevant experience.
- PharmD candidates with 1 year of experience or residency/fellowship.
- Technical Skills: MedDRA coding knowledge, familiarity with safety databases (e.g. Argus, ArisG), and pharmacovigilance regulations.
- Soft Skills: Strong keyboard skills, attention to detail, time management, and fluent verbal/written English communication.
For pharmacy professionals exploring pharmacovigilance pathways compared to conventional laboratory formulation tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Fortrea?
- Work with a leading global clinical research organization serving major pharmaceutical sponsors.
- Gain hands-on clinical trial safety management and regulatory compliance training.
- Collaborative global team environment with structured career progression.
- Continuous learning and development programs in drug safety sciences.
To test your basic knowledge of drug safety definitions, clinical trial phases, and GCP parameters before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Pharmacovigilance vs Healthcare IT
Safety Science Coordinators manage adverse event databases, write clinical patient narratives, and ensure regulatory safety reporting compliance, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Fortrea PV Candidates
- Highlight Database Experience: Clearly list any safety databases (such as Argus or ArisG) and Excel tools you used in previous roles or training.
- Specify Case Volume: Detail the volume of ICSRs processed, narratives written, or queries managed in your previous roles to show productivity.
- List Therapeutic Areas: Mention if you have experience processing safety profiles in specialized areas like oncology, immunology, or vaccines.
💬 Fortrea Safety Science Coordinator Interview Questions
- Q1. What is an Individual Case Safety Report (ICSR) and its four minimum criteria?
Answer Guidance: An ICSR reports an adverse event in an individual patient. The four minimum criteria for a valid case are: an identifiable patient, an identifiable reporter, a suspect drug product, and an adverse event. - Q2. What is MedDRA and why is it used in pharmacovigilance?
Answer Guidance: MedDRA (Medical Dictionary for Regulatory Activities) is a standardized medical terminology dictionary used to code adverse events. It allows global regulators, sponsors, and researchers to analyze safety data consistently across different regions. - Q3. How do you prioritize cases when multiple Serious Adverse Events (SAEs) are received?
Answer Guidance: I prioritize cases based on regulatory reporting timelines. For example, fatal or life-threatening unexpected ADRs must be reported within 7 calendar days, while other serious ADRs are reported within 15 calendar days.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Fortrea's official Workday career board before the deadline on July 14, 2026. Click the button below:
Apply Online – Fortrea Workday Career Board❓ Frequently Asked Questions
Q. What is the deadline to apply for this Fortrea role?
The official application deadline is July 14, 2026.
Q. What is the experience required for the Safety Science Coordinator II position?
Candidates should generally possess at least 1 year of relevant experience in pharmacovigilance or clinical safety operations.
Q. Which degrees are preferred by Fortrea for this opening?
Fortrea prefers degrees in Biological Sciences, Pharmacy, Nursing, Medical Sciences, or Life Sciences.
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