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Clinical Data Manager, External Site Studies at Jobgether. This position is posted by Jobgether on behalf of a partner company. We are currently looking for a . Clinical Data Manager, External Site Studies. in the . United States. .. As a Clinical Data Manager, you will oversee end-to-end data management for external site clinical trials, ensuring high-quality, accurate, and compliant datasets throughout the study lifecycle. You will serve as a key point of contact for Sponsors, collaborating with cross-functional teams and guiding database setup, data validation, and project timelines. This role involves training site staff, performing user acceptance testing, and maintaining data integrity across multiple systems. You will have a direct impact on the successful delivery of clinical studies, helping to accelerate the development of life-saving treatments. The position requires strong attention to detail, excellent communication skills, and the ability to manage multiple priorities in a remote work environment.. . Accountabilities. Manage clinical data for external site studies across all phases, ensuring accuracy, completeness, and compliance with regulatory and Sponsor standards.. Serve as primary Sponsor contact for data management activities and communications.. Lead the design, implementation, and validation of electronic data capture (EDC) systems.. Train site staff and client teams on EDC systems and data management processes.. Oversee CRF lifecycle, conduct user acceptance testing, and develop key study documents (Data Management Plans, Validation Plans, SAE Reconciliation Plans, etc.).. Review, clean, and reconcile clinical data, including third-party sources, and manage data queries.. Coordinate database lock and ensure timely final data delivery.. Identify potential risks, proactively resolve issues, and maintain high standards of service for internal and external stakeholders.. . Bachelor’s degree in Business, Science, or related field, or equivalent combination of education and relevant experience.. 1–3 years of industry experience in clinical data management or related functions.. Knowledge of Good Clinical Data Management Practices, GCP, ICH Guidelines, 21 CFR Part 11, and medical terminology preferred.. Familiarity with SAS and Veeva EDC preferred.. Proven ability to manage multiple projects and priorities simultaneously.. Exceptional attention to detail, organizational, and problem-solving skills.. Excellent oral and written communication skills, with ability to interact effectively across teams and with Sponsors.. Proficiency in MS Office applications and clinical data management tools.. . Company Location: United States.