Role & Responsibilities
• Validate and reconcile clinical trial data
• Perform data cleaning and query resolution
• Support database lock activities
• Ensure compliance with CDM SOPs and GCP guidelines
• Maintain study documentation
Qualification
• B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences
Experience
• 3–5 years in Clinical Data Management
Skills
• EDC systems, data validation, GCP, attention to detail, MS Excel
About the Company
Cliantha Research is a global CRO providing end-to-end clinical research services supporting international clinical trials.
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