Clinical Research Recruiter

University of Arizona

Tucson, United StatesFull time
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Location
Tucson, United States
Job type
Full time
Posted
Nov 6
Today
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About the company

University of Arizona

Higher education · 11 to 50 employees

University of Arizona on LinkedIn

What you'll do

  • Reviews clinic schedules, referrals, and recruitment lists to identify potential participants
  • Contacts prospective participants to explain study availability and assess interest
  • Reviews medical records against protocol-defined inclusion and exclusion criteria
  • Conducts screening interviews and health history reviews using established study procedures
  • Meets with prospective participants to explain study objectives, procedures, risks, benefits, and responsibilities
  • Coordinates enrollment appointments and study visits
  • Enrolls eligible participants in research databases and tracking systems
  • Creates and maintains participant research files

Key skills

RecruitmentScreening interviewsHealth history reviewsInformed consentResearch databasesTracking systems

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Read the full posting here
Recruitment: Reviews clinic schedules, referrals, and recruitment lists to identify potential participants.Contacts prospective participants to explain study availability and assess interest.Provides approved recruitment materials and study information.Tracks recruitment activities and enrollment metrics. Screening: Reviews medical records against protocol-defined inclusion and exclusion criteria.Conducts screening interviews and health history reviews using established study procedures.Collects required documentation needed to determine participant eligibility.Identifies potential eligibility concerns and escalates unusual situations to the PI or senior research staff. Informed Consent: Meets with prospective participants to explain study objectives, procedures, risks, benefits, and participant responsibilities.Answers routine participant questions regarding study participation.Ensures informed consent documents are completed accurately and filed according to study requirements.Documents the consent process in accordance with regulatory and institutional requirements. Enrollment: Coordinates enrollment appointments and study visits.Enrolls eligible participants in research databases and tracking systems.Creates and maintains participant research files.Confirms all enrollment requirements have been met prior to participation.Communicates enrollment status to study team members.

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