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and honest in the performance of all duties. Must maintain competency in regulatory and institutional requirements to conduct clinical studies in human subjects (e.g. ICH/GCP guidelines, Tri-Council
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human clinical trials of biomedical or health-related research that follows a pre-defined protocol. Trials can be industry funded, grant funded or investigator initiated. The CRU is operated by
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case the successful applicant is responsible for the accuracy, production, and control of the work unit. The successful applicant will also act a resource for junior trainees. Minimum Qualifications
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