Navatio Pharma Solutions, a leading global contract research organization specializing in pharmacovigilance, is seeking a meticulous and experienced Drug Safety Associate to join our Pharmacovigilance team as a Literature Reviewer. The ideal candidate will have 2–5 years of relevant experience in drug safety or pharmacovigilance, along with excellent communication and analytical skills.
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🔍 Key Responsibilities
- Review and process literature cases for drug safety reports.
- Ensure compliance with global pharmacovigilance regulations (GVP, ICH, FDA, EMA).
- Perform case narrative writing, MedDRA coding, and ICSR submissions.
- Collaborate with global PV teams for signal detection and risk management.
🎓 Qualifications
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
- 2–5 years of experience in pharmacovigilance or drug safety, preferably with literature review exposure.
- Strong written and verbal communication skills.
- Attention to detail and ability to work independently.
💼 Benefits
- Competitive salary ranging from ₹6,00,000 to ₹10,00,000 per annum.
- Structured training and career growth in pharmacovigilance.
- Work with global pharmaceutical clients.
- Health insurance and paid leaves.
📩 How to Apply
Interested candidates are invited to send their updated resume/CV to hr@navatiopharma.com with the subject line:
“Application for Drug Safety Associate – [Your Name]”
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