The Clinical Research Assistant II conducts standard tests in accordance with established policies and procedures. Participates in the design, administration, and execution of clinical research trials. Being a Clinical Research Assistant II ensures compliance with protocol and overall clinical objectives. Analyzes and evaluates clinical data gathered during research. In addition, Clinical Research Assistant II possesses knowledge of FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and JCAHO and International Conference on Harmonization (ICH) guidelines. Requires a ...bachelor's degree. May require ACRP or SOCRA certification. Typically reports to a manager. Being a Clinical Research Assistant II occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Working as a Clinical Research Assistant II typically requires 2-4 years of related experience.More Show Less
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Job Summary. The Clinical Research Assistant II, under the supervision of the Principal Investigator and/or senior study staff collects, processes, and enters research data in support of specified research projects. Following established protocols and procedures, they will carry out study activities and recruit and follow research subjects, as appropriate to the study objectives. Duties and Responsibilities. 1. Collects data by review of medical ...
Job Summary. The Clinical Research Assistant II, under the supervision of the Principal Investigator and/or senior study staff collects, processes, and enters research data in support of specified research projects. Following established protocols and procedures, they will carry out study activities and recruit and follow research subjects, as appropriate to the study objectives. Duties And Responsibilities. Collects data by review of medical rec...
