Informed Consent Process
Recruitment/ Study Subject Selection
Medical Terminology/Patient Medical Histories
Data Management Systems
Clinical Visit Flow - Informed Consent Process, observing visit procedures, charting, and data entry
Recruitment - using provided protocols assisting with recruitment of study subjects
Clinical Skills - blood pressures, vital signs, phlebotomy
Medical Terminology - provided with medical records to take medical histories of patients
Laboratory Skills - assist in lab procedures, operate a centrifuge, observe sample processing and shipping lab samples
Administrative Assistance in Clinical Trial Coordinating - prep charts, send certified letters, file paperwork, prepare other important study documents to assist clinical research staff
Quality Assurance - review subject charts for completion, read monitor letters and ensure visits are prepared for review, review informed consent on a trial
Clinical Trials Overview and Data Management Systems - meet department heads in Business Development, Budgets and Contracts, Accounting, IT, Recruitment, Source Document Development, and Regulatory; view data management systems and learn to enter data and answer queries
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