April Allison is a Clinical Management professional with more than 20 years of experience in the drug development and medical device industry with a strong background in global project management and clinical operations. She has global trial management and monitoring experience across a wide variety of indications, including hematology, infectious disease, immunology, oncology, ophthalmology, pediatrics, respiratory, and transfusion medicine. She is well-versed in all aspects of phase I-IV studies, from clinical development strategy and planning through closeout and submissions to regulatory authorities. April has developed protocols, consent forms, monitoring plans, case report forms, clinical study reports, SOPs, and other clinical documents related to clinical trials as well as managed a variety of third-party vendors, including CROs, IRTs, central labs, and clinical suppliers.

 

In her spare time, April enjoys traveling, reading, and spending time with friends and family