| Clinical Research Associate II |
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| Also referred to as: Clinical Research Associate II, Clinical Trials Data Analyst II, Clinical Trials Research Associate II |
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| 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. |
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| Similar Jobs: Clinical Research Associate I, Clinical Research Project Management Manager, Clinical Research Project Manager IV, Clinical Research Project Manager III, Research and Development Associate II, Clinical Research Manager, Clinical Research Project Manager II, Research and Development Associate III, Research and Development Associate IV |
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| 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 |
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| Industries: Biotechnology, Edu., Gov't. & Nonprofit, Healthcare, Pharmaceuticals | |
