Senior Manager, Clinical Data Management

Role: Associate Director of Clinical Data Management leading data quality and operational excellence across clinical studies. Responsibilities include managing CDM teams, overseeing CRO/vendor activities, resource planning, developing portfolio documents, and implementing new technologies. Ensures compliance with GCP, regulations, and standards. Requirements: 12+ years in Clinical Data Management with team leadership and project oversight experience; degree in life sciences or equivalent; proficiency with clinical database systems like Medidata Rave; strong communication and organizational skills; proactive and detail-oriented. High-Value: focus on clinical trials within biopharma, emphasizing GCP compliance, CRO oversight, and data management in a dynamic environment. Work setup: full-time roles based in Cambridge, Gaithersburg, or New Jersey, US.