Change Location

Get Salary Data on All Global Countries

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

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.

Find out Job Distribution by:
Years of Experience
Education Level
Company Size
Industry
Job Openings for Clinical Research Associate I
Job Statistics