📢 For Latest Job Updates
📲 Join WhatsApp Channel
💼 Follow on LinkedIn
Parexel Hiring Patient Safety Associate I – Freshers Welcome
Parexel
Hyderabad • Bangalore • Mohali
Freshers
Pharmacovigilance
ICSR & MedDRA
₹3.5–5.5 LPA
🏢 About Parexel
Parexel is a global CRO dedicated to advancing patient health through clinical research and pharmacovigilance excellence. The Patient Safety team supports global drug safety and regulatory compliance.
📌 Job Overview
- Role: Patient Safety Associate I
- Locations: Hyderabad, Bengaluru, Mohali
- Experience: Freshers Eligible
- Industry: Pharmacovigilance / Drug Safety
- Salary: ₹3.5 – ₹5.5 LPA (Estimated)
🔬 ICSR Processing & Case Management
- Monitor incoming safety reports
- Data entry & case processing in safety database
- MedDRA coding & case assessment
- Prepare medically cohesive narratives
- Query management & follow-ups
- Track compliance timelines
📑 Safety Reporting & Regulatory Support
- Submit ICSRs to health authorities
- Support DSUR & safety reporting
- Assist regulatory database management
- Support eCTD & xEVMPD submissions
- Risk Management Plan tracking
📚 Literature Review & Signal Screening
- Literature search & ADR identification
- Safety signal screening
- Peer review of literature abstracts
- Local journal monitoring
🎓 Eligibility & Skills
- B.Pharm / M.Pharm / Pharm.D
- Life Sciences / Biotechnology / Microbiology
- Basic pharmacovigilance knowledge
- Understanding of ICH guidelines
- MedDRA familiarity preferred
- Strong attention to detail
⭐ Why Join Parexel?
- Global CRO pharmacovigilance exposure
- Structured LMS training
- Regulatory submission experience
- Career growth into senior safety roles
- Work on global clinical development programs
🚀 Job Application Link
🛡️ Patient Safety Operations & Case Validation Screening Guide:
Parexel's global drug safety units prioritize systematic data accuracy when handling post-marketing and clinical trial safety datasets. Before validating your credentials on their direct Workday system tracking node, optimize your professional profile tracker to show foundational familiarity with Individual Case Safety Report (ICSR) coding workflows, Adverse Event (AE) seriousness validation, standard medical terminology classification, and timeline adherence for international safety compliance reporting.
Parexel's global drug safety units prioritize systematic data accuracy when handling post-marketing and clinical trial safety datasets. Before validating your credentials on their direct Workday system tracking node, optimize your professional profile tracker to show foundational familiarity with Individual Case Safety Report (ICSR) coding workflows, Adverse Event (AE) seriousness validation, standard medical terminology classification, and timeline adherence for international safety compliance reporting.
.png)
