CRA II - Central / Midwest U.S. Region

This position can be home-based in the following states Texas Oklahoma Kansas Missouri Indiana Illinois Iowa Nebraska North Dakota South Dakota Michigan Minnesota or Wisconsin. The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices FDA guidelines local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites....read moreApply NowCompany

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