To support ongoing clinical research efforts, the full-time Clinical Data Manager will oversee the collection, processing, and management of clinical trial data, ensuring accuracy and compliance with regulatory requirements while working remotely. Key responsibilities Develop and maintain data management plans, validation specifications, and study-related documents Oversee the setup, validation, and maintenance of electronic data capture systems and perform data cleaning and issue resolution activities Coordinate with CROs and vendors to ensure timely and compliant data activities while maintaining documentation for inspection readiness Required qualifications Bachelor's Degree in Life Sciences, Health Information Management, Computer Science, or a related field 4-6 years of experience in clinical data management, preferably in pharmaceutical, CRO, or biotech settings Proficiency in EDC systems such as Medidata Rave, Veeva, and InForm Familiarity with data standards such as CDISC, MedDRA, and WHODrug Experience with database lock processes and query management
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