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📄 Position:
- 🏢 Company: Navitas Life Sciences
- 📍 Location: Chennai
- 🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
- 🧑💼 Experience: 0–2 years in Clinical Data Management (CDM)
- 📌 Job Type: Full-Time | Verified Job | Online Application
🏢 About Company:
Navitas Life Sciences is a global clinical research organization (CRO) headquartered in Princeton, NJ, with over 1,000 employees across 5 countries. The company accelerates life-saving therapies through technology-driven clinical data management, regulatory services, and end-to-end CRO solutions.
As part of HIG Portfolio, Navitas provides:
- ✔ Data Science & Clinical Trial Optimization
- ✔ Regulatory & Safety Compliance
- ✔ Functional Service Provider (FSP) Solutions
📝 Job Overview:
Position: Clinical Data Coordinator
🧩 Responsibilities:
- Review Case Report Form (CRF) data for accuracy, completeness, and consistency.
- Perform Medical Coding using MedDRA & WHODRUG dictionaries.
- Conduct Quality Reviews and resolve data discrepancies.
- Generate and manage data queries for clinical trials.
- Assist in database testing, edit checks, and validation.
- Perform SAE (Serious Adverse Event) reconciliation.
- Ensure compliance with clinical data management (CDM) procedures.
- Prepare study documentation and status reports.
🎯 Eligibility & Skills:
- Bachelor’s/Master’s in Life Sciences, Pharmacy, or related field.
- Freshers with internship experience in CDM may apply.
- ✔ Proficiency in MedDRA & WHODRUG coding
- ✔ Strong attention to detail & data accuracy
- ✔ Knowledge of GCP, ICH guidelines, and clinical trials
- ✔ Familiarity with EDC (Electronic Data Capture) systems
🎁 Why Join:
- ✅ Competitive salary (Not Disclosed)
- ✅ Career growth in a global CRO
- ✅ Exposure to cutting-edge clinical trials
- ✅ Work in Chennai, a major pharma hub
📝 Application Link:
🔒 Please wait 15 seconds. Application link will appear here.
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