Clinical Research Associate II

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Clinical Research Associate II participates in the design, administration, and execution of clinical research trials. Conducts standard tests in accordance with established policies and procedures. Being a Clinical Research Associate II analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Additionally, Clinical Research Associate II possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Requires a bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. The Clinical Research Associate II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Clinical Research Associate II typically requires 2-4 years of related experience.