Clinical Research Associate I

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Clinical Research Associate I participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Being a Clinical Research Associate I ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. Additionally, Clinical Research Associate I may require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. The Clinical Research Associate I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Clinical Research Associate I typically requires 0-2 years of related experience.