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Hiring Patient Safety Associate I & Clinical Operations Assistant
🏢 Parexel
📍 Mohali & Mumbai
⏳ 0–1 Years
💊 Pharmacovigilance & Clinical Research
Parexel is hiring freshers for two high-demand roles in Pharmacovigilance (PV) and Clinical Operations. If you're confused between domains, check 👉 Healthcare IT vs Clinical Career Guide
📌 Patient Safety Associate I (Mohali)
This role is focused on drug safety & pharmacovigilance, where you handle adverse event data and ensure patient safety.
Key Responsibilities:- ICSR (Individual Case Safety Report) processing
- MedDRA coding & case triage
- Adverse Drug Reaction (ADR) analysis
- Case narrative writing
- Literature review for safety signals
- Regulatory submissions (FDA, EMA guidelines)
- Basic knowledge of Pharmacovigilance
- Understanding of MedDRA & ICSR workflow
- Good medical writing skills
- Attention to detail
📌 Clinical Operations Assistant (Mumbai)
This role focuses on clinical trial coordination and documentation, supporting global clinical studies.
Key Responsibilities:- Maintain Trial Master File (TMF)
- Update CTMS systems
- Coordinate with investigator sites
- Support site activation & trial execution
- Ensure ICH-GCP compliance
- Understanding of clinical trials
- Knowledge of TMF & CTMS
- Strong coordination skills
- Documentation accuracy
💰 Salary & Career Growth
- ₹3 – ₹6 LPA (Freshers)
- PV Path: Safety Associate → PV Scientist → Manager
- Clinical Path: CTA → CRA → Clinical Project Manager
- Salary Comparison Guide
💡 General Interview Tips
- Clear basics of GCP & clinical trials
- Understand difference between PV & Clinical roles
- Practice aptitude 👉 Aptitude Quiz
- Read 👉 Interview Guide
🚀 Job Application Links (Parexel)
🚀 Apply Now: Patient Safety Associate I (Mohali)
🚀 Apply Now: Clinical Operations Assistant (Mumbai)
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core skills align with pharmacovigilance operations, adverse event case tracking, clinical trial management systems (CTMS) support, trial master file (TMF) documentation, and ICH-GCP regulatory guidelines compliance before proceeding.
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core skills align with pharmacovigilance operations, adverse event case tracking, clinical trial management systems (CTMS) support, trial master file (TMF) documentation, and ICH-GCP regulatory guidelines compliance before proceeding.
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