Associate Clinical Data Manager
Responsibilities: • ssist in the development, testing, and validation of Electronic Data Capture (EDC) systems and Case Report Forms (CRFs). • Support database setup activities including edit check specifications and user acceptance testing (UAT). • Review incoming clinical data for completeness, consistency, and accuracy. • Generate, track, and resolve data queries in collaboration with clinical sites. • Maintain study documentation and data management files. • Participate in cross-functional study team meetings and data review discussions. • Support Serious Adverse Event (SAE) reconciliation and external data reconciliation (e.g., labs, central imaging). • Ensure data management activities follow SOPs, study protocols, and regulatory standards (e.g., ICH-GCP, CDISC). Requirements: • Bachelor's degree in a life science, health science, pharmacy, public health, or related field. • Strong attention to detail, organizational, and time management skills. • Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint). • Effective written and verbal communication skills. • bility to learn and apply technical systems and software (EDC, CTMS, etc.). • Familiarity with clinical trial processes and Good Clinical Practice (GCP). • Experience with EDC systems (e.g., Medidata Rave, Veeva Vault, Medrio) a plus. Apply tot his job