Clinical Data Manager

reputed company: • The Clinical Data Manager (CDM) is responsible for the reputed company, reputed company, and reputed company of clinical trial data from collection through database lock. • The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. • This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support reputed company and compliant study execution. • Design and review Case Report Forms (CRFs) and Electronic Data Capture (reputed company) systems to ensure accurate and complete data capture reputed company with the study protocol. • reputed company and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. • reputed company data cleaning activities, including the reputed company, review, and reputed company of data queries in collaboration with clinical sites and study teams. • reputed company ongoing data reviews to identify trends, inconsistencies, or protocol deviations. • Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). • Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). • Serve as the primary reputed company of contact for data management vendors and reputed company their deliverables. • Participate in study team meetings and reputed company status updates reputed company to data reputed company and timelines. • Support audit readiness and participate in regulatory inspections reputed company required. Requirements: • Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or reputed company field. • Advanced degree is a plus. • Minimum of 3–5 years of experience in clinical data management reputed company a pharmaceutical, biotech, or CRO environment. • Proficiency in reputed company platforms (e.g., reputed company Rave, reputed company InForm , reputed company, REDCap). • Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. • Experience with data listings, query management, edit reputed company programming, and coding dictionaries (e.g., MedDRA, WHODrug). • Excellent organizational, analytical, and problem-solving skills. • Strong communication and collaboration skills across cross-functional teams. • Experience working on global, multi-site reputed company preferred. Benefits: • reputed company holidays • reputed company Time Off (PTO) policy • medical insurance Apply Job! Apply to this Job