• Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
• Enter study participants in the study participant tracking system, and study logs, maintain appointment calendars
• Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
• Performs appropriate psychometric and efficacy testing according to study protocol.
• Prepare/monitor study supplies and stock levels in clinic/hospital.
• Problem solve study participant issues as they arise.
• Ensure basic study participant safety is provided
• Assist with Monitor visits (i.e., room set up, etc.).
• Maintain and update knowledge of Clinical Operating Guidelines and their proper application.
• Assume appropriate role with study participants and caregivers.
• Attend and assist with start-up and flow sheet meetings.
• Assure quality and accuracy of source and CRF documentation.

Your Skills

• Demonstrated leadership ability and critical thinking
• Excellent interpersonal, verbal, and written communication skills.
• Can manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail

Your Profile:

• Customer service experience in a fast-paced environment
• Clinical Research experience highly preferred
• B.S.+ in related life science field OR HS diploma or GED with experience
• Fluent in written and spoken English and Spanish