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Ontario Clinical Research Associate I Salaries

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• Job Description for Clinical Research Associate I
  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.

  Alternate Job Titles: Clinical Trails Research Associate I,Clinical Trials Data Analyst I
  Categories: Pharmaceuticals , Biotechnology , Entry Level , Science and Research