Clinical Trial Management Post-master鈥檚 Certificate
Students have the option to complete a post-master鈥檚 curriculum in clinical trial management in 51动漫鈥檚 offered through the school鈥檚 .听
This post-master鈥檚 certificate requires the completion of coursework focusing on the tools and information needed to understand how clinical trials must be designed and overseen in the pharmaceutical industry, including writing protocols and consent forms, delving into the requirements of good clinical practices, and managing budgets and data. To apply for this 15-credit program, applicants must hold a master鈥檚 degree in a pharmacy-related field and a bachelor of science degree in biochemistry, biology, chemistry, physics or a health-related discipline.
Learning Objectives
Upon completion of the post-master鈥檚 certificate, students will understand the
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basis for new drug discovery;
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design and implementation of the clinical protocol, its conduct and effective monitoring strategies;
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auditing of data to ensure the integrity of the trial;
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bioethics of clinical research;
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protection of the human research subject;
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informed consent form and process; and
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role and responsibilities of the key personnel鈥攖he IRB, sponsor, monitor, CRO and the clinical investigator.