Skip to main content

This job has expired

PS Study Coordinator

Employer
University of Utah
Location
Utah, United States
Salary
Salary Not specified
Date posted
Apr 29, 2024

View more



PS Study Coordinator

Job Summary

The Division of Pediatric Endocrinology at the University of Utah has an immediate opening for a Study Coordinator to join our dynamic Clinical Research Team. This position offers the opportunity to be part of an expanding clinical research team studying ways to improve the lives of children with chronic diseases. The study coordinator will manage the technical and administrative details involved in a clinical research study and assist the Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.
The University of Utah offers a comprehensive benefits package including:
Additional benefits information is available at https://benefits.utah.edu/

Responsibilities
  1. Assesses protocol for clarity and subject safety, reviews inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and sponsor.
  2. Attends and participates in Investigator and staff meetings. Advises team regarding specific study assignments and timelines.
  3. Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety.
  4. Determines length of visits and coordinates related facility and equipment availability.
  5. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor.
  6. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor as needed across our various Endocrine and Diabetes related studies.
  7. Completes, audits, corrects CRFs, relays CRFs to sponsor.
  8. Assists with negotiating contract budget and payment terms.
  9. Maintains documents as required by FDA guidelines.
  10. Maintain contact with IRB and prepare and submit IRB documents.
  11. Ensure proper collection, processing and shipment of specimens.
  12. Perform functions required of the Clinical Research Assistant as necessary.


Problem SolvingIncumbents are responsible for coordinating the daily operations of their assigned research team, coordinating the orderly and safe flow of the research project and maintaining adequate resources for the PI to accomplish their research objectives.CommentsWork Environment and Level of Frequency that may be requiredNearly Continuously: Office environment.Physical Requirements and Level of Frequency that may be requiredNearly Continuously: Sitting, hearing, listening, talking.Often: Repetitive hand motion (such as typing), walking.Seldom: Bending, reaching overhead.The staff member must be able to demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served on his or her assigned unit. The individual must demonstrate knowledge of the principles of life span growth and development and the ability to assess data regarding the patient’s status and provide care as described in the department’s policies and procedures manual.


Minimum Qualifications
Bachelor’s degree in a related field, or equivalency (one year of education can be substituted for two years of related work experience) required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire and demonstrated human relations and effective communication skills are also required.

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. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.

Some departments may require IATA DGR training within six months.

Preferences
Previous clinical research experience. Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; attention to detail; and the ability to function independently is preferred. Excellent interpersonal and communications skills, both oral and written. Proficiency in Microsoft Office and ability to learn new software programs.Phlebotomy certification or previous Phlebotomy experience is preferred.Candidates will be screened according to preferences.

Special Instructions


Requisition Number: PRN38380B
Full Time or Part Time? Full Time
Work Schedule Summary: Monday - Friday, 8 am - 5 pm.
Department: 00848 - Pediatric Administration
Location: Campus
Pay Rate Range: $38,300 - $55,621
Close Date:
Open Until Filled: Yes

To apply, visit https://utah.peopleadmin.com/postings/163859


jeid-9866afa24c3a4244bb4f7e124e22b9c0

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert