Clinical Research Coordinator II: Data Management & Compliance
McLaren USA
McLaren in Michigan is seeking a Study Coordinator/Data Management/Regulatory Specialist to provide support to the Clinical Trials Office. This full-time role requires managing independent assignments and ensuring compliance with clinical trial protocols. The ideal candidate will have a Bachelor’s degree, preferably with medical/science education, and will engage in various responsibilities including data management, maintaining logs, and coordinating site visits. #J-18808-Ljbffr
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- ...responsible for : Manages all operational aspects... ...implementation of one or more clinical trials and all... ...the study protocol and coordinates completion of QC... ...Technology (IRT), Electronic Data Capture (EDC), eDiary... ...files to ensure their compliance with required...DataContract workRemote work
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