Robyn Bell Email and Phone Number

• Assist various Principal Investigators/Physicians, through delegated authority, in conducting trials per Federal, State and Institutional guidelines. • Collected accurate Vital signs.• Responsible for all phases of trials including pre-study implementation through study closure, which includes maintaining of clinical research files and related documents. • Review protocols and other materials provided by Study Sponsors in order to give input to the Principal Investigators and Manager regarding clinical applicability and feasibility. • Responsible for coordinating the implementation of various protocols for assigned research projects with the appropriate departments, providing in-service education for healthcare professionals, and working with the Pharmacy. • Design, build, and update spreadsheets and other tracking tools. • Complete IRB continuing review reports, and assist with drug accountability. Coordinate study monitoring visits, data analysis, compile and submit manuscripts, abstracts, and other documents for publication as appropriate.• Conducts Clinical Research Trials including Start up, Phase I, II and III protocols, and close-out, by using the following Electronic Data Capture (EDC) systems: • MyTrials, InForm, LABCONNECT, IWRS/IVRS. • Serves as a liaison between patients, physicians, and study sponsors. • Manages numerous subject visits without supervision which included obtaining ECG, vitals and collection of laboratory specimens.• Prepares and shipped to the Lab in Pursuant with Regulations, in addition to the disbursement of subject visit payments while keeping an accurate record of via Clinical Conductor.