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Essential Job Duties:

In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed. Responsibilities may include but are not limited to:

• Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol:
• Assists with the basic screening of patients for study enrollment;
• Assists with patient follow-up visits;
• Documents in source clinic charts;
• Enters data in EDC and answers queries;
• Obtains vital signs and ECGs;
• May perform blood draws;
• Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
• Request and track medical record requests;
• Enters data in EDC and answers queries;
• Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and
• Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;
• Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
• Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;
• Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and
• Perform all other duties as requested or assigned.