Maurice Hardy

About Maurice Hardy

I started off my career as a Officer in the US Navy before joining the industry as a Clinical Research Associate where I specialize in overseeing clinical trials, ensuring their quality and progress.My background includes a Board Certification in Medical Affairs as well as experience in surgery, electronic medical record systems, and leadership. I am fueled by a dedication to advance healthcare through innovative research and technology, and carry out this dedication using my problem-solving abilities, effective communication, and commitment to evidence-based medicine that are recognized by my peers. I aim to make a significant impact through the above traits in addition to my research and clinical expertise.

Experience

1. Clinical Research Associate

   Ppd

   Nov 2022 — Present

   Successfully managed and completed Site Management Contacts (SMCs) for the clients’ studies, adhering strictly to the timeline and ensuring preparation for the Data Base Lock (DBL) with proactive engagement with KOLs in obtaining Principal Investigator (PI) signatures well in advance of the deadlines for assigned studies.Successfully managed sites as an on-site monitor completing Interim Monitoring Visits for clients’ studies, adhere strictly to timelines earning the commendations of clinical trial managers and sponsor representatives.Exemplified strong independent working capabilities by securing necessary PI signatures for 21 sites in the client’s study, facilitating an early database lock and surpassing scheduled targets.Facilitated the Close Out Visit (COV) process through meticulous document collection, significantly contributing to the timely DBL in both assigned studies.Earned commendation from Clinical Trial Manager (CTM) for exceptional site preparation and diligent daily query resolution, demonstrating a high level of follow-up and support.Demonstrated strong therapeutic knowledge, contributing to team efforts as a collaborative team player with a proven ability to communicate effectively both orally and in writing.Played a key role contributing to a second client’s study by showing initiative and sharing expertise as a Clinical Trial Coordinator (CTC), praised for being a solid performer and for seamlessly integrating into the team during a critical Interim Analysis phase.Progressively trained in different roles that include Clinical Trial Coordinator, Assistant Clinical Research Associate, and Clinical Research Associate roles prior to entering the Clinical Research role full time.Over 2 year of monitoring solid tumor trials, rare disease, neuroscience, and general medicine trials as a Clinical Research Associate.

Education

• State University of New York at Oswego

  Master of Science - MS, Bioinformatics

• Loma Linda University

  Doctor of Medicine (M.D.)

  2011 — 2015

• Andrews University

  Bachelor of Science (B.S.), Biology, General

  2007 — 2011