Also referred to as: Clinical Trails Research Associate II, Clinical Trials Data Analyst II
Requirements and Responsibilities

Clinical Research Associate II participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Being a Clinical Research Associate II ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. Additionally, Clinical Research Associate II 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 II occasionally directed in several aspects of the work. Gains 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.

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