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Senior Clinical Trial SpecialistKforce Clinical Research Staffing - Thousand Oaks, CAUnder direct supervision of the CTM or Senior CTM, coordinates and monitors the activities associated with the evaluation, initiation and management of clinical trials. This person coordinates activities performed by CROs and ensures timely and quality management of clinical trials. Major Duties and Responsibilities: * Monitors clinical studies for adherence to protocol, GCP and company SOPs; ensures timely enrollment against plan * Ensures quality of data generated from clinical sites and assists in resolving patient eligibility and protocol deviation issues * Confirms the accuracy of administrative data * Ensures adverse events are reported properly and follow-ups done in a timely manner * Prepares study documents (consents, site instructions, etc.) * Assists in the design, format, and content...originally from Kforce Clinical Research Staffing - More Tools...
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