Fortrea Hiring Safety Science Coordinator I in Pune
Fortrea is hiring for the position of Safety Science Coordinator I at its Pune location. This is an excellent opportunity for freshers and candidates with up to 1 year of experience in pharmacovigilance or clinical safety.
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Fortrea Hiring Safety Science Coordinator I in Pune📍 Job DetailsKey Responsibilities🔹 Safety Reporting & Case Processing🔹 Regulatory & Compliance🔹 Data Management & Quality🔹 Coordination & Support🎓 Eligibility Criteria✔️ Educational Qualification✔️ ExperienceRequired SkillsWhy Join Fortrea?📌 How to ApplyAPPLY HERE
The role focuses on handling adverse event (AE/SAE) processing, safety reporting, and regulatory compliance within clinical trials and post-marketing environments.
📍 Job Details
- Position: Safety Science Coordinator I
- Location: Pune, India
- Job Type: Full-Time
- Job ID: 26879
- Last Date to Apply: April 11, 2026 (Apply ASAP – limited time left)
Key Responsibilities
🔹 Safety Reporting & Case Processing
- Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
- Perform data entry of AE/SAE cases into safety databases
- Write patient narratives and perform MedDRA coding
- Handle listedness assessment for marketed products
🔹 Regulatory & Compliance
- Submit SAE reports to regulatory authorities, clients, and ethics committees
- Ensure compliance with global safety regulations and timelines
- Maintain safety documentation and tracking systems
🔹 Data Management & Quality
- Maintain and update adverse event tracking systems
- Perform quality review and reconciliation of safety databases
- Generate queries for missing or inconsistent data
🔹 Coordination & Support
- Support project teams and safety personnel
- Schedule meetings and maintain project documentation
- Train and mentor junior team members
- Assist in archiving safety study files
🎓 Eligibility Criteria
✔️ Educational Qualification
Candidates from the following backgrounds are eligible:
- B.Pharm / M.Pharm / PharmD
- Life Sciences / Biological Sciences / Nursing / Medical Sciences
✔️ Experience
- Freshers to 1 year of experience in:
- Pharmacovigilance (PV)
- Clinical Safety
- Regulatory Affairs / Clinical Data Management
Required Skills
- Strong attention to detail
- Good written & verbal communication
- Basic knowledge of MS Office & data handling
- Ability to manage multiple tasks
- Team player with problem-solving skills
Why Join Fortrea?
- Work with a leading global CRO organization
- Exposure to clinical trials & pharmacovigilance
- Career growth in drug safety & regulatory domain
- Opportunity to work on international projects
📌 How to Apply
Interested candidates can apply directly through the official Fortrea careers portal using Job ID 26879.
👉 Apply immediately as the deadline is very close!

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