✅ Novartis – Clinical Project Associate & Regulatory Affairs Executive (0–5 Yrs)
🏢 Company: Novartis📍 Location: Hyderabad & Mumbai
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
🧪 Experience: 0 – 5 Years (Both Entry-Level & Experienced)
📝 Job Type: Full-Time | Onsite | Clinical Research & Regulatory Affairs
🔎 Verified: ✅ Verified Opportunity
🧬 About Novartis
Novartis is a global pharmaceutical leader committed to reimagining medicine and improving lives. Known for innovation, inclusivity, and research excellence, Novartis offers employees a purpose-driven work culture, career growth, and global opportunities.📄 Job Overview
Openings:1️⃣ Clinical Project Associate – Hyderabad
2️⃣ Executive – Regulatory Affairs – Mumbai
🧑💼 Key Responsibilities
Clinical Project Associate:- Assist in study documentation, CSR appendices, TMF maintenance
- Support trial supply management, data review, meeting coordination
- Track clinical trial drug shipments and expiry
- Assist in vendor coordination, finance forecasting, and compliance
- Handle submissions: NDAs, CTAs, PSURs, renewals
- Coordinate with HA, QA, legal, and supply chain
- Support clinical trials from a regulatory perspective
- Maintain compliance with regulatory intelligence and CAPA plans
✅ Skills & Qualifications
- Degree in Pharmacy / Life Sciences (PG preferred for RA role)
- Clinical trials, CTMS tools, regulatory documentation
- Strong communication & collaboration across teams
- 0–2 years for Clinical Associate, 3–5 years for RA Executive
🎁 Why Join Novartis?
- 🚀 Work on cutting-edge global clinical trials
- 🌐 MNC culture with flexible policies
- 💼 Great benefits, growth & exposure
- 🤝 Inclusive, supportive global teams
📌 Note Before You Apply:
Update your resume with relevant experience in CROs or document management systems. Tailor your application to highlight coordination and compliance experience in clinical operations.
👇 Select Location & Role to Apply 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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