Leading data management activities for early phase clinical pharmacology studies, the full-time Senior Clinical Data Manager will oversee complex studies, collaborate with cross-functional teams, and ensure timely, accurate data management to support safety reviews and study conduct in a remote environment. Key responsibilities Manage and monitor data management activities and vendor relationships for assigned studies Lead the design and testing of Electronic Data Capture (EDC) systems and ensure compliance with data capture requirements Provide mentorship and training to junior Data Management staff while participating in process improvement initiatives Required qualifications At least five years of experience in Data Management within the pharmaceutical/biotechnology industry, including two years leading Phase I studies Comprehensive understanding of regulatory guidelines and industry standards related to Data Management Strong project management skills with the ability to prioritize multiple tasks effectively Experience in supporting Phase I Healthy Volunteer clinical pharmacology studies BA/BS degree, preferably in a scientific or healthcare field
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