Clinical Research Associate I
Also referred to as: Clinical Research Associate I, Clinical Trails Research Associate I, Clinical Trials Data Analyst I
Requirements and Responsibilities
Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. 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. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.
Similar Jobs:  Clinical Research Associate II, Research and Development Associate I, Research and Development Associate V, Research and Development Associate III, Research and Development Associate IV, Scientist - Clinical Research, Research and Development Associate II, Clinical Research Director, Clinical Research Manager
Level of Education:  Clinical Research Associate I Salaries with a Bachelor's Degree, Clinical Research Associate I Salaries with a Master's Degree or MBA, Clinical Research Associate I Salaries with a JD, MD, PhD or Equivalent
Industries:  Biotechnology, Edu., Gov't. & Nonprofit, Healthcare, Pharmaceuticals