The Clinical Research Assistant I conducts standard tests in accordance with established policies and procedures. Participates in the design, administration, and execution of clinical research trials. Being a Clinical Research Assistant I ensures compliance with protocol and overall clinical objectives. Analyzes and evaluates clinical data gathered during research. In addition, Clinical Research Assistant I possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Requires a bac ...helor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Assistant I work is closely managed. Works on projects/matters of limited complexity in a support role. Working as a Clinical Research Assistant I typically requires 0-2 years of related experience.More Show Less
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