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CRA III (32859) Company Name: MedFocus Prepare and independently performs study site qualification, initiation, interim monitoring, and close-out visits at the clinical investigative sites to ensure adherence to protocol, procedures, and project plans in accordance with FDA regulations. Maintain site files, trial master files and study documentation. Activities and oversight to support the operational execution of clinical trial procedures, ensuring high quality, accuracy and integrity of data reported. May be. After registering you may be able to apply for this job directly (if still active) on ((None))'s site. Future job matches may be sent from Geebo approved job partners.
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