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Safety Science Coordinator I
Fortrea
Pune
0–2 Years
Pharmacovigilance
Drug Safety
₹3.5–5.5 LPA
📅 Last Date to Apply: 3 March 2026
🏢 About Fortrea
Fortrea is a global CRO providing clinical development, safety, and regulatory solutions. The organization supports pharmaceutical and biotech companies worldwide.
📌 Job Overview
- Role: Safety Science Coordinator I
- Location: Pune
- Experience: 0–2 Years
- Department: Clinical Safety / Pharmacovigilance
- Job ID: 26589
- Salary: ₹3.5 – ₹5.5 LPA (Estimated)
🔬 Pharmacovigilance & Safety Processing
- Process AE/SAE cases in safety databases
- Prepare patient safety narratives
- MedDRA coding & listedness assessment
- Submit expedited safety reports
- Maintain adverse event tracking systems
📑 Regulatory & Compliance Support
- Support regulatory submissions
- Assist database reconciliation
- Ensure SOP & QMS compliance
- Maintain safety documentation & archives
🎓 Eligibility & Skills
- B.Pharm / M.Pharm / PharmD
- Life Sciences / Biological Sciences / Nursing
- 0–2 years PV or clinical research experience
- Knowledge of AE/SAE & MedDRA preferred
- Strong attention to detail & communication skills
⭐ Why Join Fortrea?
- Strong entry into pharmacovigilance career
- Global drug safety exposure
- Work on regulatory safety reporting
- Career growth in CRO safety operations
📌 Note Before You Apply:
Candidates with pharmacovigilance training or knowledge of AE/SAE processing will have an advantage.
Candidates with pharmacovigilance training or knowledge of AE/SAE processing will have an advantage.
🚀 Job Application Link
🛡️ Safety Science Operations & PV Screening Guide:
Fortrea's drug safety monitoring infrastructure evaluates analytical talent profiles based on meticulous tracking within post-marketing and clinical safety pipelines. Before deploying your candidate metrics onto their Workday system network, optimize your resume keywords to emphasize structural baseline understanding of Adverse Event (AE) case validation, standard MedDRA coding taxonomy, safety narrative processing log maintenance, and global pharmacovigilance regulatory compliance standards.
Fortrea's drug safety monitoring infrastructure evaluates analytical talent profiles based on meticulous tracking within post-marketing and clinical safety pipelines. Before deploying your candidate metrics onto their Workday system network, optimize your resume keywords to emphasize structural baseline understanding of Adverse Event (AE) case validation, standard MedDRA coding taxonomy, safety narrative processing log maintenance, and global pharmacovigilance regulatory compliance standards.
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