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Title Clinical Research Associate
Target Location US-NJ-Trenton
Email Available with paid plan
Phone Available with paid plan
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Candidate's Name ,MDWest State Street Apt 2,Trenton NJ Street Address . tel :PHONE NUMBER AVAILABLE EMAIL AVAILABLESummaryA Clinical Research Associate with entry-level experience, specializing in quality control, audits, continuous improvement, and GCP regulations. Adept at analyzing complex data sets and identifying opportunities to enhance the quality of clinical research initiatives.Professional ExperienceClinical Research Associate professional Fastrack programJuly 2022  PresentWrote clinical trial documentation for a pharmaceutical company analyzing the efficacy of a new antidepressant, including consent forms, study protocols, and QC guidelinesEnsure compliance with FDA, ICH, and GCP regulations, conduct study audits, develop SOPs, and identify opportunities to reduce protocol deviationsCoordinate with research coordinators to ensure the accuracy and transparency of dataClinical Research Internship, Fastrack programMay 2022  August 2022Provided support for the planning and execution of clinical studies under the direction of the CRA, including reviewing documentation and driving process improvementsEnsured compliance with ethical and scientific standards for data collection and analysisEducationTrainee clinical Research professional july 2022 Fastrack programDiploma Medical Doctor in sept 2000 Universite Detat DHaitiKey SkillsClinical ResearchGCP RegulationsClinical Trial DocumentationProcess ImprovementQuality ControlCertificationsCertified Clinical Research Associate (CRA), ACRA, 2022

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