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 Description: Clinical Data Coordinator
Key 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.
Skills & Experience Required:
✔ 0-2 years in Clinical Data Management (CDM)
✔ 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
Eligibility & Benefits
Eligibility Criteria:
- Bachelor’s/Master’s in Life Sciences, Pharmacy, or related field.
- Freshers with internship experience in CDM may apply.
Employee Benefits:
✅ Competitive salary (Not Disclosed)
✅ Career growth in a global CRO
✅ Exposure to cutting-edge clinical trials
✅ Work in Chennai, a major pharma hub
How to Apply?
