Description
Summary: * Screened potential subjects for protocol eligibility. Presented trial details to subjects, participated in the informed consent process, and enrolled subjects into studies * Increased patient satisfaction ratings by timely follow-ups on patients' health status and ensured subject compliance with the study protocol * Accelerated participant enrollment through effective data collection, documentation and managing the initial clinical tests. * Served as the primary liaison between investigators, clinical staff, and research subjects. * Improved turnaround time by preparation & coordination of lab samples and the shipments. * Knowledge of statistical analysis and epidemiological approaches * Respond to requests/queries from investigative sites in a timely fashion * Assisted with preparation of IRB applications, including protocol and informed consents and obtaining approval to conduct the study. * Maintained source documents and regulatory documentation of clinical trial. Ensured quality of data on CRFs
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