Prescreen Coordinator I

ALLIANCE CLINICAL LLCLas Vegas, NV
9h

About The Position

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!

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.

Nice To Haves

  • Associate’s degree in healthcare or related field, preferred.
  • Certified Medical Assistant or related field, preferred.
  • 2 years’ experience in running research protocols, preferred.
  • 2 years’ experience in FDA regulations and GCP, preferred.

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.
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