The goal of this position is to assist the Clinical Trials Department with the maintenance of several complex ongoing clinical trials with a focus on patient-specific responsibilities. Responsible for the following aspects of the Clinical Trials process including but not limited to: Lead CRA coordinating study activities, monitoring of study compliance, maintenance of electronic data systems (EDC) to ensure accurate data entry, ensuring patient safety, study start-up procedures, consenting patients, monitoring patients on trials and toxicity assessment under direction of the principal investigator, maintaining and updating study databases, entering patient's visit in the Clinical Trials Management System (CTMs), overseeing processing/storing/shipping of lab specimens, ethics submission and ongoing regulatory monitoring and trial procedures. Exercises considerable independent judgement and decision making, using broadly defined policies, practices and procedures, to resolve a variety of complex problems.
Education: * 4-year Undergraduate Degree in Health Science - required or recognized equivalent of education and experience
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