Physicians' Research Options, LLC, operating Medical Clinics in Utah, Colorado and Nevada, is seeking a CRC/CCRC/CCRP for our Women's Health Clinic in Draper, UT. All research operations are conducted from dedicated research offices within the clinic(s).
The primary function of the Clinical Research Coordinator is to coordinate the conduct of clinical research protocols in the in-hospital (occasional) and clinic settings (primary) with an emphasis on the regulatory paperwork, recruitment, screening, enrollment, subject health, conduct of protocol visits, data collection, data entry, correspondence with Investigators and Sponsors, and monitoring of patient candidates/participants.
Associate’s Degree in a Healthcare or Clinical Research related field required; Bachelor’s Degree in a Healthcare or Clinical Research related field preferred;
Other Medical/Clinical experience
Minimum three (3) years of practical work experience acceptable in lieu of education.
Minimum of one (1) years of research experience for qualified candidates
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP), preferred; or willing to attain.
Proficient in word processing, computer spreadsheets, mainframe computer applications, and database management.
Ability to prioritize and organize a high volume workload and changing priorities.
Familiar with principles of protocol implementation, study design, statistics, applicable regulations, and IRB process.
Phlebotomy and lab sample processing preferred.
Valid driver's license and reliable transportation required.
Other requirements apply.
Additional Salary Information: Wage commensurate with education and research trial experience.