• Obtain and maintain informed consent, study participant education, study enrollment, data quality management, obtain blood samples, collect specimens, perform vital signs, review medical history, maintain/create source documentation, and schedule patients for follow up visits• Conduct and document daily Direct Observed Therapy (DOT) visits for study participants.• Frequently review DOT log for accurate documentation and compliance• Review DOT doses given to study participants• Maintain electronic binders

• Initiated, managed and monitored various clinical research projects and provided project specific administrativesupport• Scheduled and participated in monitoring and auditing activities• Conducted independent study coordination and screening of potential patients for protocol eligibility• Coordinated laboratory samples and compiled data• Prepared and executed clinical studies according to good clinical practice guidelines. Create necessary paperwork.• Log in test materials.• Prepare dilutions.• Prepare study rooms for the next day's studies (including material stocking and room cleanup).• Score irritation and/or other attributes of the skin. Provide courteous service to panelists and clients.