Senior Clinical Data Associate

Roles & Responsibilities
• Support Lead Data Manager and act as backup for end-to-end CDM activities
• Perform CRF review, specifications development, and database build/UAT support
• Conduct clinical data review, query management, and line listing reviews
• Perform medical coding and AE/SAE reconciliation
• Maintain data management documentation with version control
• Coordinate with EDC vendors and third-party stakeholders
• Support database lock, metrics reporting, and process improvements
• Train study teams on CRF, EDC, and study-specific processes

Qualification
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Computer Applications, or related discipline

Experience
• Relevant experience in Clinical Data Management within a CRO or sponsor setup
• Hands-on experience across the clinical trial lifecycle

Skills
• Strong experience with EDC systems (Medidata Rave, Veeva Vault preferred)
• Good knowledge of ICH-GCP and clinical trial processes
• Experience in medical coding, data review, and database lock
• Strong analytical, documentation, and communication skills

About the Company
Precision For Medicine is a global CRO focused on precision medicine and advanced clinical research, delivering innovative data-driven solutions to accelerate drug development across complex and rare diseases.