AstraZeneca Careers India: Clinical Trial Safety Scientist Role | ICH-GCP | Pharmacovigilance | Bengaluru





💼 AstraZeneca Hiring: Scientist – Clinical Trial Safety | Bengaluru | 2–6 Years


🏢 Company: AstraZeneca
📍 Location: Bengaluru (Hybrid)
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences, Nursing, BDS, Medicine, PhD, Veterinary Science
🧪 Experience: 2–6 Years (Clinical Trials / PV / Safety Data Review)
💰 Salary: Competitive (Industry Standard)
📝 Job Type: Scientist – Clinical Trial Safety | Full-Time | Global R&D
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in

📄 Job Overview

AstraZeneca is hiring Scientist – Clinical Trial Safety for its Bengaluru location. This role supports the Trial Safety Review Center (TRISARC) focusing on global clinical trial data review, safety assessments, patient safety insights, and ICH-GCP compliant documentation.


🔬 Key Responsibilities

  • ✔ Assist Senior Scientists with study setup & documentation.
  • ✔ Review patient-level safety & clinical trial data.
  • ✔ Generate safety queries for high-quality medical assessments.
  • ✔ Prepare visualizations, study reports & presentations.
  • ✔ Maintain TRISARC documents in eTMF & perform quality checks.
  • ✔ Manage trackers, SharePoint, study tools & communication mailboxes.
  • ✔ Support meeting schedules, documentation & improvement initiatives.


✅ Essential Qualifications

  • 🎓 BSc/MSc/PhD in Life Sciences, Nursing, Pharmacy, Medicine, Dentistry, Veterinary Science.
  • 📘 Strong understanding of ICH-GCP, SAE reporting & clinical data review.
  • 🧠 Excellent communication, analytical & documentation skills.
  • 💻 Strong computer proficiency and multitasking skills.

✨ Desirable Experience

  • ✔ Prior experience in clinical trials or pharmacovigilance.
  • ✔ Experience reviewing SAEs / safety data.
  • ✔ Understanding of clinical data flow & drug development.
  • ✔ Basic programming exposure (bonus).


🎁 Why Join AstraZeneca?

  • 🌍 Work in a world-recognized R&D environment.
  • 💊 Contribute to life-changing medicines & global clinical trials.
  • 🏢 Hybrid work model (minimum 3 days onsite).
  • 🤝 Collaborative, inclusive, diverse workplace culture.
  • 📈 Cross-functional learning & growth opportunities.

For more Job 👇👇


📌 Note Before You Apply:
Update your CV with clinical trial safety, SAE review, ICH-GCP knowledge to improve interview shortlisting.


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🟢 Verified Job via Medical Jobs India – hitechplus.in

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