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Clinical Research AssociateCleveland, OH1) Liaise with Compliance staff and perform site audits 2) Ensure that site personnel are conducting the study in accordance with ICH/GCP guidelines 3) Perform CRO/CRA assessment to ensure they are meeting expectations as defined in the SOPs 4) Ensure that principal investigator complies with SAE reporting requirements as defined by applicable SOPs and regulatory authorities 5) Perform ongoing on-site data management and collection to ensure that issues regarding quality of data are communicated to the site personnel Job Requirements: 1) Bachelor?s degree in a scientific discipline or RN 2) 5+ years of experience in clinical trial 3) Experience in the medical device industry as a monitor 4) Experience in CNS therapeutic (stroke preferred) 5) Experience in site and CRO auditing 6) Willingness...originally from The Job Spider - More Tools...
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