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.
This role is ideal for candidates with 1–4 years of experience in clinical data management, eCRF handling, and UAT testing, looking to work in a regulated, GCP-compliant environment.
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Key Responsibilities – 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:
- 1–4 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: ₹4 LPA – ₹7.5 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
