Will Young Email & Phone Number

Responsibilities include monitoring clinical trials to ensure sponsor and investigator obligations are being met and activities are compliant with applicable local regulatory requirements and ICH guidelines. Also, conducting site visits sites to assess the qualification of potential investigative sites, initiate studies, instruct site personnel on the proper conduct of studies, to review data and ensure accuracy of data collected and to terminate studies. Performing source document verification, reviewing drug accountability and safety and documenting deviations to protocol and regulations at investigative sites, as well as reviewing Serious Adverse Event (SAE) reporting for compliance with regulations/specifications. Mentoring junior team members and reviewing trip reports has been an ongoing responsibility.Specialties: Neurology, Nephrology, Neuroscience, Infectious Disease, Oncology, ESRD, Psychiatry, Respiratory, Reproductive/Women's Health, Cardiovascular, Psoriatic Arthritis, Endocrinology.

Listed skills include Clinical Monitoring, Clinical Trials, Endocrinology, Nephrology, and 7 others.

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  East Carolina University

  Communications