A strong opportunity is available for professionals looking to build a career in Clinical Data Management (CDM) with Aithent in Chennai.
Although originally labeled as a Clinical Research Associate (CRA) role, the responsibilities clearly align with a Clinical Data Management / Clinical Data Associate profile, focusing on clinical trial data handling, validation, and system testing.
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This role is ideal for candidates with 1โ4 years of experience in clinical data management, eCRF handling, and UAT testing, looking to work in a regulated, GCP-compliant environment.
Key Responsibilities โ Clinical Data Management (CDM)
- Ensure accuracy, consistency, and integrity of clinical trial data
- Perform data review, cleaning, and query generation in eCRF systems
- Raise and resolve data discrepancies with study teams
- Conduct User Acceptance Testing (UAT) for clinical systems and applications
- Support clinical database validation and system workflows
- Maintain and review data management documentation and tracking tools
- Assist in preparation of Data Management Plans (DMPs) and data manuals
- Collaborate with clinical operations, programming, and data teams
- Ensure compliance with ICH-GCP, protocols, and SOPs
- Generate clinical data reports and study progress summaries
Qualifications & Skills
Education:
- B.Pharm / B.Tech (Biotech / Biochemistry)
- M.Pharm (preferred)
Experience:
- 1โ4 years in Clinical Data Management / Clinical Research
Required Skills:
- Strong knowledge of ICH-GCP guidelines
- Hands-on experience with eCRF / EDC systems
- Exposure to UAT testing and validation processes
- Good understanding of clinical trial data lifecycle
- Strong analytical and documentation skills
Salary & Benefits
- Estimated Salary: โน4 LPA โ โน7.5 LPA
- Exposure to global clinical trial data systems
- Opportunity to work in clinical data validation & UAT
- Growth path into:
- Clinical Data Analyst
- Data Management Lead
- Clinical Systems Specialist
How to Apply
