PS Clinical Research Coord

Job Summary

Responsibilities

Qualifications

Skills

Benefits

Pay

Schedule

• Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
  • Develops study budgets; monitors budget expenses and billing for allied services; negotiates payment schedule with sponsor and fees for internal services.
  • Maintains enrollment goals and initiates strategies to promote enrollment and participant compliance.
  • Captures and reports adverse events and protocol deviations.
  • Captures and reports adverse events and protocol deviations.
  • Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.
  • Represents the research program at meetings, national and international research consortia.
  • Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence.
  • Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues.
  • Supervises, mentors and trains new or junior research staff.
  • Coordinates with referring physicians to provide information regarding available research projects and to maintain a strong referral basis.
  • Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
  • Aids the Principal Investigator in the development of study protocols.

Problem Solving: Decides how to best accomplish the daily requirements of various study objectives, prioritizes and delegates workload and establishes systems needed to achieve specific study goals. Efforts of multiple departments or disciplines must be coordinated to ensure effective follow through and compliance of all involved. Functions independently under minimal supervision, following FDA, Good Clinical Practice, IRB, NIH, NCI, NSF and/or other regulatory agency guidelines and seeks council from the Principal Investigator as necessary. Functions independently under minimal supervision, following FDA, Good Clinical Practice, IRB, NIH, NCI, NSF and/or other regulatory agency guidelines and seeks council from the Principal Investigator as necessary. Functions independently under minimal supervision, following FDA, Good Clinical Practice, IRB, NIH, NCI, NSF and/or other regulatory agency guidelines and seeks council from the Principal Investigator as necessary.

Qualifications

• Bachelor’s degree in a health sciences or related field or equivalent (one year of education can be substituted for two years of related work experience).
• Two years professional research experience.
• Completion of University RATS Clinical Certification within one year of hire required.
• Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills.
• Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently is preferred.
• Departments may require IRB CITI Course or IATA DGR training within a specified timeframe.
• Departments may prefer a nursing degree for this position, which requires the incumbent to have two years related experience and possess a nationally recognized research compliance certification.
• This position is patient-sensitive and must fulfill all associated requirements.
• We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy.
• Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
• Preferences: Special Instructions Requisition Number: PRN44753B Full Time or Part Time? Full Time Work Schedule Summary Department: 01167 - HCI Clinical Trials Operations Location: Campus Pay Rate Range: 39300 to 72700 Close Date: 7/15/2026 Open Until Filled To apply, visit https://utah.peopleadmin.com/postings/200266 Copyright ©2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-1f47a8e21190034c92a0ef569ec07c6a