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💼 Thermo Fisher Hiring: Safety Administrator (Pharmacovigilance) | Freshers Eligible | Remote (India)
🏢 Company: Thermo Fisher Scientific (PPD)
📍 Location: Remote, India
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences or relevant degrees
🧪 Experience: 0–1 Years (Freshers can apply)
💰 Salary: ₹4.3 – ₹6.2 LPA (approx.)
📝 Job Type: Safety Administrator | Full-Time | Pharmacovigilance | Remote
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🏢 About Thermo Fisher Scientific (PPD)
Thermo Fisher Scientific’s PPD clinical research business is a global leader in life sciences and clinical development. Join a mission-driven team that supports drug safety and regulatory excellence worldwide while offering flexible, remote work opportunities.
📄 Job Overview
Thermo Fisher (PPD) is hiring Safety Administrators to support the Global Safety Writing Team. You will help organize safety documentation, coordinate communications, and ensure timely, compliant delivery of aggregate reports, regulatory responses, and Risk Management Plan (RMP) components.
🔬 Key Responsibilities
- ✔ Manage team mailbox and ensure quick, accurate routing of communications.
- ✔ Track team/project information and maintain compliance metrics.
- ✔ Schedule meetings, prepare planning docs, and support data requests for authors.
- ✔ Format, compile, and quality-check final safety deliverables.
- ✔ Maintain organized filing and document control for safety submissions.
- ✔ Work to strict timelines to meet regulatory and project deadlines.
✅ Required Qualifications & Skills
- ✅ B.Pharm / M.Pharm / Pharm.D / MSc / BSc / Life Sciences (or relevant degree).
- ✅ 0–1 year experience; pharmacovigilance/clinical research exposure is a plus.
- ✅ Strong MS Word & Excel skills; fast and accurate typing.
- ✅ Excellent English communication, grammar, and attention to detail.
- ✅ Ability to prioritize, multitask, and adapt to evolving processes in a remote setup.
🎁 Benefits of Joining Thermo Fisher (PPD)
- 🏠 100% Remote (India) with collaborative global teams.
- 📈 Career growth in Pharmacovigilance & Clinical Research.
- 🗂 Exposure to aggregate safety reports, RMPs, and regulatory deliverables.
- 💼 Work with a world leader in life sciences and drug development.
📌 Note Before You Apply:
Tailor your CV to highlight MS Word/Excel proficiency, document formatting, pharmacovigilance basics, and meeting coordination to improve shortlisting chances.
👇 Apply Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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