✅ Clinical Trial Specialist Job – Emerald Clinical Trials
🏢 Company: Emerald Clinical Trials📍 Location: Hybrid – Bangalore
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
🧪 Experience: 2–3 Years
📝 Job Type: Full-Time | Clinical Research | TMF | Regulatory
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🧬 About Emerald Clinical Trials
Emerald Clinical Trials is a full-service CRO with expertise in renal, cardiometabolic, and oncology trials. Headquartered in APAC, Emerald blends global reach with local insights to accelerate clinical development.📄 Job Overview – Clinical Trial Specialist
- 📌 Job Title: Clinical Trial Specialist (Hybrid)
- 📌 Location: Bangalore, India
- 📌 Department: Clinical Operations
🧑💼 Key Responsibilities
- Maintain and QC Trial Master File (TMF) – eTMF and hardcopy
- Support IRB/EC regulatory submissions and ICF documentation
- Oversee site feasibility, start-up, and essential documents
- Update Clinical Trial Management System (CTMS)
- Assist with audits and ensure ICH-GCP compliance
✅ Eligibility & Skills
- 2–3 years in clinical research or as CTS
- Bachelor's or Master’s in Life Sciences, Pharmacy, or Nursing
- Knowledge of ICH-GCP, regulatory process, TMF systems
- Organized, detail-oriented, with strong communication
🎁 Benefits at Emerald
- 🌐 Global trial exposure & APAC/US studies
- 💻 Hybrid work options (office + remote)
- 📈 Mentorship & learning culture
- 🏥 Work-life balance & wellbeing programs
📌 Note Before You Apply:
Highlight your TMF, GCP, and regulatory document experience. Tailor your CV to clinical trial operations.
👇 Application Link Will Be Visible After Countdown 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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