✔ Verified by Medical Jobs India
Safety Science Analyst
Pune
0–1 Years
Pharmacovigilance
Drug Safety
Clinical Safety
🏢 About Fortrea
Fortrea is a global Contract Research Organization (CRO) specializing in clinical development, pharmacovigilance, and regulatory services for pharmaceutical, biotechnology, and medical device companies. The organization supports global clinical trials and safety monitoring programs to ensure patient safety and regulatory compliance.
📌 Job Overview
- Role: Safety Science Analyst
- Company: Fortrea
- Location: Pune, India
- Experience: 0–1 Year
- Employment Type: Full-Time (6 Month Contract)
- Department: Pharmacovigilance / Clinical Safety
🔬 Key Responsibilities
- Perform case intake and triage of incoming safety reports
- Process adverse event cases according to pharmacovigilance procedures
- Enter safety data into adverse event tracking systems
- Write patient narratives and perform MedDRA coding
- Conduct listedness assessments against product labels
- Generate queries for incomplete safety information
- Submit expedited SAE reports to regulatory authorities
- Assist with periodic safety reports and regulatory submissions
- Support database reconciliation for safety systems
- Maintain documentation according to SOPs and quality standards
- Assist with archiving safety case documentation
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D
- BAMS / BDS / BHMS
- Nursing Degree
- 0–1 year experience in pharmacovigilance or clinical safety
- Knowledge of MedDRA coding or adverse event reporting is an advantage
- Strong attention to detail
- Good communication and documentation skills
- Basic proficiency in MS Office tools
⭐ Career Growth Opportunities
- Exposure to global pharmacovigilance systems
- Hands-on experience in clinical safety databases
- Opportunity to work with international clinical development teams
- Career growth into roles like:
- Drug Safety Associate
- Pharmacovigilance Scientist
- Clinical Safety Specialist
- Aggregate Reports Analyst
- Regulatory Safety Specialist
💰 Salary (Estimated)
- ₹3.5 LPA – ₹6 LPA (Based on industry standards)
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Basic understanding of pharmacovigilance processes, adverse event reporting, and MedDRA terminology will increase your chances of being shortlisted.
Kindly read the entire job description carefully before applying. Basic understanding of pharmacovigilance processes, adverse event reporting, and MedDRA terminology will increase your chances of being shortlisted.
👇 Apply Online 👇
⏳ Apply link unlocks in:
15
.png)
