Prescreen Coordinator I

Pre-Screening Coordinator The Pre-Screening Coordinator is responsible for coordinating and overseeing site screening schedules, managing pre-screening operations and overseeing patient eligibility assessments. If you are a motivated professional with a passion for clinical research and patient engagement, we invite you to apply! Essential Duties And Responsibilities: Review and breakdown protocols and informed consents for patient eligibility and recruitment. Conduct prescreen visits and assessments. Must have excellent organizational, attention to detail, interpersonal skills, and possess a high level of multi-tasking capacities. Maintain a thorough understanding of various research study guidelines that include both inclusion and exclusion criteria. Explain the study procedures and answer questions to ensure that potential participants understand the study requirements and process. Explain the study's purpose, procedures, risks, benefits, compensation and follow up care to potential participants prior to entry into the study. Perform screening exams on participants to determine their health status prior to participating in studies involving new medications or procedures. Create and maintain detailed records of all call logs and study candidates including their names, addresses, phone numbers, birth dates and other identifying information. Collect and analyze test results from candidates to determine if they have any physical impairments that could interfere with their participation in the study. Oversee site screening schedules, ensuring all activities adhere to compliance requirements. Coordinate performance and time efficiency in the prescreen visit flow. Comply with all company policies, procedures, and conduct. Strictly adhere to confidentiality and compliance standards. Qualification Requirements: Associate's degree in healthcare or related field, preferred. Certified Phlebotomy Technician (CPT) license required. Certified Medical Assistant or related field, preferred. 2 years' experience in running research protocols, preferred. 2 years' experience in FDA regulations and GCP, preferred. Proven track record of analytic reasoning skills and problem solving. Exceptional attention to details and organization. Must possess excellent verbal and written communication skills. A proven ability to multi-task in a rapidly changing environment. Location: Las Vegas, NV Worker Category: Temporary

Created: 2026-03-10