✅ IQVIA Hiring Safety Aggregate Report Specialist – Apply Now (1–3 Yrs, Bangalore & Thane)
🏢 Company: IQVIA📍 Location: Bangalore & Thane (Onsite)
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences or related
🧪 Experience: 1 – 3 Years
📝 Job Type: Full-Time | Pharmacovigilance | Drug Safety | Safety Reports
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🧬 About IQVIA
IQVIA is a global leader in advanced analytics, clinical research, and technology solutions for the life sciences industry. With operations in over 100 countries, IQVIA accelerates healthcare innovations and drives impact across the clinical trial and pharmacovigilance landscape.
📄 Job Overview – Safety Aggregate Report Specialist
- Author and review safety aggregate reports (PBRERs, DSURs, PSURs, PADERs, ACOs, etc.).
- Conduct signal detection, validation, and documentation activities.
- Perform literature surveillance for ICSRs, events of interest, and inclusion in reports.
- Collaborate with regulatory teams and respond to agency queries.
- Mentor junior staff and contribute to project metrics and process improvements.
✅ Eligibility & Skills
- Bachelor’s degree (Life Sciences or equivalent); Master’s preferred
- 1–3 years experience in PV, signal management, or aggregate reporting
- Knowledge of ICH-GCP, pharmacovigilance regulations, and MedDRA coding
- Strong communication, QC review, multitasking and organizational skills
- Experience with ARGUS, ArisG, and Microsoft Office tools
🎁 Why Join IQVIA
- 🌐 Global exposure to diverse pharmacovigilance projects
- 📈 Career growth & mentorship programs
- 💼 Competitive salary and employee benefits
- 🧠 Work on impactful, patient-centered safety reports
📌 Note Before You Apply:
Review the key responsibilities and required skills carefully before applying. Tailor your resume for better shortlisting chances.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
.jpg)
.jpg)
){kind=link}
0 Comments