🧪 eTMF & CTMS Specialist – Job Details 💻
📌 Job Role
- eTMF & CTMS Specialist
🧑💼 Experience
- 3–4 Years in Clinical Research
🎓 Qualification
- B.Pharm / M.Pharm / Life Sciences / Clinical Research 🎓
💼 Key Responsibilities
- Manage eTMF systems & document filing 📂
- Handle CTMS modules (site tracking, payments, milestones) 📊
- Ensure ICH-GCP compliance ✅
- Maintain audit-ready documentation 🔍
- Coordinate with Clinical Ops, QA & Data teams 🤝
🛠️ Required Skills
- Hands-on experience in eTMF (Veeva Vault etc.) 💻
- Knowledge of CTMS platforms
- Understanding of TMF & ALCOA+ principles
- Strong regulatory & documentation knowledge
🌟 Benefits
- High-demand clinical research role 🚀
- Exposure to global trial systems 🌍
- Career growth in Clinical Operations & QA 📈
📩 How to Apply
- Send CV to: rahulkumar.cr@merillife.com 📧
- Subject: Application for eTMF & CTMS Specialist – Pharmabharat
👉 Great opportunity for experienced clinical research professionals 👍
