Michael Gabriel Md Email & Phone Number

Sarasota, Florida, United States

• Ensure Good Clinical Practice (GCP) compliance and accurate data verification.• Perform routine monitoring visits, manage data queries, and ensure the integrity of trial data.• Oversee the execution of monitoring plans, preparing reports, and resolving site issues.• Provide site training and support.• Facilitate technology support and ensure sites have access to necessary materials and information. • Effective communication abilities to convey complex information clearly and liaise between site staff and the research team• Attention to detail, flexibility in managing multiple priorities and adapting to changing project needs.• Comfortable using clinical trial management systems and addressing basic technology issues, with the ability to escalate more complex problems appropriately.

Ogden, Utah, United States

Senior Clinical research coordinator site support focusing on Influenza and Covid vaccines, lung cancer, hypercholesterolemia, Asthma, and colorectal cancer studies. As CRC, provide clinical research support to investigators to prepare for and execute assigned research studies, includingreview study protocols, Case Report Forms (CRFs), other study specific documents, and electronic datacapture system used to record clinical research data.Responsible for attending all relevant study meetings. Collect and submit regulatory/ethicsdocumentation as required by relevant regulatory bodies governing the conduct of clinical research.Recruit and screen patients for clinical trials and maintain subject screening logs.Orient research subjects to the study as needed, including the purpose of the study, procedures, andprotocol issues such as timelines for visits.Maintain source documentation based on protocol requirements. Schedule and execute study visits andperform study procedures.Collect, record and maintain research subject study data according to study protocol and SOPs,preserving quality control for content, accuracy and completeness.Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics.Monitor subject safety and report adverse reactions to appropriate medical personnel. Correspond withresearch subjects and troubleshoot study-related questions or issues.Assist with study data quality checking and query resolution.Perform a variety of complex clinical research procedures including but not limited to ECG, samplecollection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.Record, report and interpret study findings appropriately to develop a study-specific database.Assist investigator in verifying that research study objectives are met on time, within budget andaccording to all applicable protocol requirements, clinical research regulations and quality standards.