Cliantha Research is hiring a Clinical Data Associate (CDA) for its Ahmedabad location. This opportunity is ideal for professionals with 2–6 years of experience in Clinical Data Management (CDM) who are skilled in EDC studies, data validation, SAE reconciliation, and medical coding.
As a Clinical Data Associate at Cliantha Research, you will work closely with Study Leads and cross-functional clinical teams to ensure high-quality, compliant, and timely clinical trial data delivery.
This role offers strong exposure to end-to-end data management activities in a reputed Contract Research Organization (CRO).
🧪 Key Responsibilities – Clinical Data Associate
As part of the Clinical Data Management team, your responsibilities will include:
- Coordinating with Study Leads to ensure smooth study progress
- Creating and maintaining Data Management Plans (DMPs) and Data Validation Plans (DVPs)
- Designing and reviewing CRFs for paper and EDC studies
- Performing UAT based on edit checks and database specifications
- Ensuring consistency between CRFs and data entry screens
- Training clinical sites on EDC systems and managing role-based access
- Identifying and resolving data discrepancies through manual and system checks
- Performing data management QC for assigned studies
- Generating, updating, and verifying DCF and Ex-DCF queries
- Managing and reconciling external data (labs, vendors, etc.)
- Conducting SAE reconciliation
- Performing medical coding of CRF terms
- Ensuring compliance with SOPs, work instructions, and project scope
- Maintaining training documentation and study records
- Collaborating with Programmers, Statisticians, CRAs, Monitors, and external teams
- Supporting study close-out and archival activities as per SOPs
🎓 Eligibility & Qualifications
Education:
- UG: B.Pharm (any specialization)
- PG: M.Pharm / M.Sc / MS (any science specialization)
Experience:
- 2 to 6 years of relevant experience in Clinical Data Management
Key Skills:
- Clinical Data Management (CDM)
- EDC systems & database handling
- Data validation & discrepancy management
- SAE reconciliation
- Medical coding
- CRF design (paper & EDC)
- External data reconciliation
- SOP & GCP compliance
💼 Why Join Cliantha Research?
- Work with a globally recognized clinical research organization
- Exposure to end-to-end CDM lifecycle
- Strong SOP-driven and quality-focused environment
- Collaborative cross-functional clinical teams
- Career growth in clinical research & data management
📍 Job Location
Ahmedabad, Gujarat, India
💰 Salary (Expected)
₹6,00,000 – ₹10,00,000 per annum
(Salary is indicative and may vary based on experience and interview performance)
📝 How to Apply?
