📢 For Latest Job Updates
📲 Join WhatsApp Channel
📢 Join Telegram Channel
💼 Follow on LinkedIn
✔ Verified by Medical Jobs India
Hiring Pharmacovigilance & Regulatory Roles
🔥 Last Date for PV Role: 26 April 2026
🏢 Parexel
📍 Hyderabad / Remote
⏳ 3–6+ Years
📊 PV / Regulatory
Parexel is hiring for two roles: Pharmacovigilance (PV) and Regulatory Affairs. This is a great chance to work in a global clinical research company.
💊 Pharmacovigilance – Patient Safety Specialist
- Location: Hyderabad
- Experience: 3–6 Years
- Last Date: 26 April 2026
- Work on ICSR case processing
- Write safety narratives
- Review ADR (adverse drug reaction)
- Follow ICH and global safety rules
- Use safety databases (Argus etc.)
👉 Practice before applying: PV Quiz
📄 Regulatory Affairs Associate
- Location: Remote (Bengaluru)
- Experience: 5+ Years
- Work on eCTD submissions
- Prepare regulatory documents
- Follow US FDA guidelines
- Manage regulatory projects
👉 Learn basics: Regulatory Guide
💡 Interview Tips
- Revise ICH-GCP basics
- Understand ICSR process
- Know basic regulatory steps
- Prepare simple real examples
- Practice Quiz
📄 Resume Tips
- Use keywords: ICSR, PV, eCTD
- Add tools like Argus
- Keep resume simple (1–2 pages)
- Highlight your experience clearly
❓ FAQ
- Can freshers apply?
No, experience is required - Is this remote?
RA role is remote - Salary?
₹5–18 LPA (approx)
📌 Note Before You Apply:
Kindly read the full job details carefully before applying. Make sure your experience matches the role. Applying carefully increases your chances of selection.
🚀 Job Application Links (Parexel)
🚀 Apply Now: Patient Safety Specialist (Pharmacovigilance Role)
🚀 Apply Now: Senior Regulatory Affairs Associate (Regulatory Affairs Role)
📌 Important Note Before You Apply:
Kindly read the full job details carefully for your selected role before applying. Ensure your profile, qualifications, and core skills align with patient safety surveillance, adverse event reporting, global regulatory submissions, or pharma compliance documentation workflows before proceeding.
Kindly read the full job details carefully for your selected role before applying. Ensure your profile, qualifications, and core skills align with patient safety surveillance, adverse event reporting, global regulatory submissions, or pharma compliance documentation workflows before proceeding.
.png)
