Ms. Cleaver is a Director of Clinical Affairs at MCRA with over 17 years of experience in the industry.
Ms. Cleaver received her Bachelor of Science in Human Biology/Exercise and Health from Oxford Brookes University in 2000.
Prior to joining MCRA in July 2018, Ms. Cleaver worked at Sucampo Pharmaceuticals, Inc. in Rockville, MD as the Director of Clinical Operations where she acquired an in-depth knowledge of the full lifecycle of drug development, inclusive of protocol development, site selection and management, timeline and budget management, data analysis for global Phase I-IV studies. Ms. Cleaver can be relied upon to leverage her experiences to drive process improvement, increasing performance, GCP, and regulatory compliance. Throughout her professional career she has been recognized for leading cross-functional teams to ensure optimal alignment of site operations, data monitoring and review, and safety surveillance and reporting.
Ms. Cleaver is a results-driven and forward-thinking clinical operations professional. At MCRA, Ms. Cleaver provides operational leadership for the design, planning, and implementation of studies, primarily for orthopedic devices.