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Hiring Patient Safety Associate I
Parexel
Hyderabad / Mohali
Freshers
Pharmacovigilance
🏢 About Parexel
Parexel is a leading global CRO providing clinical development and regulatory services. It offers strong exposure to pharmacovigilance, drug safety, and global clinical trials.
📋 Job Overview
- Role: Patient Safety Associate I
- Location: Hyderabad / Mohali
- Experience: Freshers
- Domain: Pharmacovigilance / Drug Safety
- Job Type: Full-Time
📌 Key Responsibilities
- ICSR case processing & data entry
- MedDRA coding & narrative writing
- Adverse event monitoring & reporting
- Case follow-ups & reconciliation
- Regulatory submissions & compliance
- Literature screening & signal detection
🎓 Eligibility Criteria
- M.Sc / M.Pharm / PharmD / BDS
- Life Sciences / Biomedical graduates
- Pass-out: 2023–2026
💻 Skills Required
- Basic pharmacovigilance knowledge
- ICSR & AE reporting understanding
- ICH guidelines basics
- Good communication skills
- Attention to detail
💰 Salary & Benefits
- ₹3.5 – ₹5.5 LPA
- Global clinical trial exposure
- Training & learning programs
- Career growth in PV
📚 Internal Resources
🎯 Interview Tips
- Understand ICSR workflow
- Revise MedDRA basics
- Practice AE case scenarios
- Focus on PV regulations
📌 Note Before You Apply:
Read full job requirements carefully before applying. PV basics are important for selection.
Read full job requirements carefully before applying. PV basics are important for selection.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile and core qualifications align with pharmacovigilance operations, adverse event (AE) case processing, safety data management, medical coding (MedDRA), global safety reporting timelines, and ICH-GCP regulatory compliance guidelines before proceeding with your application on the Parexel portal.
Kindly read the full job description carefully before applying. Ensure your profile and core qualifications align with pharmacovigilance operations, adverse event (AE) case processing, safety data management, medical coding (MedDRA), global safety reporting timelines, and ICH-GCP regulatory compliance guidelines before proceeding with your application on the Parexel portal.
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