The Clinical Trials Data Analyst I analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trials Data Analyst I knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trials Data Analyst 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. Being a Clinical Trials Data Analyst I wor ...k is closely managed. Works on projects/matters of limited complexity in a support role. Working as a Clinical Trials Data Analyst I typically requires 0-2 years of related experience.More Show Less
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