Best clinical trial design
Certificate registration is required to complete the program. Candidates are encouraged to register in the certificate program as early as possible to take advantage of program benefits. See Certificate FAQs for more information.
The three required courses have no substitutes, and cannot be waived. Recommended: The Drug Development Process to be taken first, after any prerequisites.
Those pursuing the Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRA) credentials through ACRP, or the Clinical Research Professional (CCRP) credentials through SoCRA, can fulfill educational requirements by completing this program. For information about ACRP certification, please go to . For more information about SoCRA certification, please go to .
Barbara Bigby, MA
Lynne Eddy, PhD
Angela McMahill, JD, CHRC, CHC, CCRA
David Shapiro, M.D.
Robin Smith, RN, BSN, CCRA
Daniel Szpak, RN, CCRC
David Tanen, MD
Keith Vaux, MD
Leonel Villa-Caballero, MD, PhD
Terence Webb, PharmD, MBA
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What is academic researcher perspective on CRO involvement in clinical trials?
To me, it is a positive step which allows the scientist to spend more time engaged in mastering his discipline at a deep level, rather than the formalism of the experiments that he wants to conduct.