Clinical Research Associate II
Also referred to as: Clinical Research Associate II, Clinical Trials Data Analyst II, Clinical Trials Research Associate II
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 master's degree in science or equivalent. Typically reports to a supervisor or manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience.
Similar Jobs:  Clinical Research Associate I, Clinical Research Manager, Research and Development Associate II, Research and Development Associate I, Research and Development Associate III, Research and Development Associate IV, Research and Development Associate V, Scientist - Clinical Research, Clinical Research Director
Level of Education:  Clinical Research Associate II Salaries with a Bachelor's Degree, Clinical Research Associate II Salaries with a Master's Degree or MBA, Clinical Research Associate II Salaries with a JD, MD, PhD or Equivalent
Industries:  Biotechnology, Edu., Gov't. & Nonprofit, Healthcare, Pharmaceuticals