Clinical Research Associate III
Also referred to as: Senior Clinical Research Associate, Clinical Research Associate III
Requirements and Responsibilities
Participates in the design and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. May evaluate each clinical phase for study. May assist in developing clinical processes and procedures. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. May require a bachelor's degree of Science, Science in Nursing, RN or its equivalent. Typically reports to a supervisor or manager. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. Typically requires 4 to 7 years of related experience.
Job Statistics
Years of Experience Education Level
Company Size Industry
Similar Jobs:  Clinical Research Associate III - Biotech, Clinical Research Associate II, Clinical Research Associate I, Research and Development Associate III, Research and Development Associate IV, Research and Development Associate V, Research and Development Associate I, Research and Development Associate II, Clinical Research Associate I - Biotech
Level of Education:  Clinical Research Associate III Salaries with a Bachelor's Degree, Clinical Research Associate III Salaries with a Master's Degree or MBA, Clinical Research Associate III Salaries with a JD, MD, PhD or Equivalent
Categories:  Pharmaceuticals, Biotechnology, Science and Research
Industries:  Biotechnology, Edu., Gov't. & Nonprofit, Healthcare, Pharmaceuticals,
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