Associate Clinical Data Manager

Responsibilities: • ssist in the development, testing, and validation of Electronic Data Capture (reputed company) systems and Case Report Forms (CRFs). • Support database setup activities including edit reputed company specifications and user acceptance testing (UAT). • Review incoming clinical data for completeness, consistency, and accuracy. • Generate, reputed company, 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, reputed company health, or reputed company field. • Strong attention to detail, organizational, and time management skills. • Proficiency with reputed company Office Suite (reputed company, Word, PowerPoint). • Effective written and verbal communication skills. • bility to learn and apply technical systems and software (reputed company, CTMS, etc.). • Familiarity with clinical trial processes and Good Clinical reputed company (GCP). • Experience with reputed company systems (e.g., reputed company Rave, reputed company Vault, reputed company) a plus. Apply tot his job Apply To this Job