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Role & Responsibilities
• Lead data review and discrepancy management
• Coordinate database lock activities
• Mentor junior CDM staff
• Ensure compliance with regulatory standards
Qualification
• B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences
Experience
• 5–6 years in Clinical Data Management
Skills
• Advanced EDC handling, leadership, query management, documentation
About the Company
Cliantha Research is a global CRO offering clinical development, bioanalytical and regulatory services.