Senior Clinical Data Manager

Role: Senior Clinical Data Manager leading data management efforts within Ocugen's clinical development programs and marketed products. Responsibilities: oversee study data collection, database design, CRF development, data validation, and quality assurance; lead cross-study consistency; mentor junior staff; manage vendors; ensure compliance with GCP, ICH, CDISC standards; support audit readiness and documentation; collaborate with Clinical Operations, Biostatistics, and Regulatory teams; develop data strategies and standards; author SOPs and DMPs; participate in cross-functional project planning. Requirements: BS in sciences, nursing, or related; 5-7 years clinical data management experience in biopharma or CRO; strong knowledge of GCP, ICH, FDA, CDISC; experience with EDC systems (Veeva preferred), CRFs, IRT; excellent organizational, communication, and problem-solving skills; detail-oriented; capable of working in fast-paced environment. HighValue: clinical trials, data management, GxP compliance, EDC/database design, audit readiness, cross-functional collaboration. WorkSetup: primarily office-based with limited remote work; may require outside hours for business needs.