Matt holds the ACRP-CP and CCRC certifications through ACRP and is a member of SCRS, ACRP, MAGI, and SoCRA. He has over 15 years of experience in clinical research on both the site and sponsor level. On the site side, Matt has worked as a study coordinator, site manager, director of clinical research, and assists sites with budget/contract negotiation, accounts receivable management, and regulatory affairs including ISF oversight and administration. On the sponsor side, he’s gained knowledge and experience in monitoring, clinical operations, finance/accounting, TMF management, and has drafted and revised several protocols for Parkinson’s disease and provided insight for protocols for Alzheimer’s disease, autism, hallucinations, multiple system atrophy, and schizophrenia, as well as assisting sponsors with the feasibility process, site identification, site selection, and site payments.
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