Reproductive Psychiatry Research Program (RPRP), brainchild of Dr. Jennifer L. Payne is seeking to add a Clinical Research Coordinator (CRC) to the team. The goals of the studies conducted at RPRP is to understand the genetic, biological and psychological causes of the reproductive related mood disorders.

The Clinical Research Coordinator will work on a Department of Defense sponsored single site study, prospective, longitudinal study. Aim of the study is to develop a blood/saliva test which is predictive of postpartum depression. The blood or saliva test is still investigational and not FDA approved. This is remote study where 1000 participants will be recruited from all over the country.

Job Responsibilities:

Work closely with an experienced CRC and/or Principal Investigator to learn the full scope of clinical research duties. Learn how to read and follow a clinical trial protocol as it is written.Demonstrate a clear understanding of the importance of patient safety in clinical research and identify the components of a clinical trial protocol that are employed to protect patient safety.Engage in the following study conduct activities: recruitment, prescreen and identify eligible patients, screen, obtain and document informed consent, enroll subjects in a study and follow up until the end of the study.Manage ongoing study conduct activities such as: coordinate study visits, maintain concomitant medication records, track and report adverse events, organize subject study payments.Collect and enter study data in a timely fashion, maintain corresponding documentation.Collect, process, store and ship study specimens as needed.Assist in preparation and maintenance of existing study documentation such as: study visit schedules, study drug diaries, monitoring and or training logs, equipment records or study communications.Prepare basic regulatory documentation to the IRB such as: annual protocol continuations, and minor protocol modifications.Become familiar with the various electronic platforms utilized in clinical research such as: IRB Pro, Protocol Builder, CRConnect, OnCore, Epic, REDCap, EDC, Payment Work.Demonstrate a continuously increasing level of clinical research knowledge gained through active participation in training and mentorship opportunities as well as self-guided learning.In addition to the above job responsibilities, other duties may be assigned.

MINIMUM REQUIREMENTS

Clinical Research Coordinator, Non-Licensed 

Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications.

Experience: None. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.

Licensure: None.

Clinical Research Coordinator, Licensed

Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse.

Experience: None.

Licensure: Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.

PHYSICAL DEMANDS
This is primarily a sedentary job involving extensive use of desktop computers. The job does occasionally require traveling some distance to attend meetings, and programs.

Salary will be commensurate with education and experience.

This is a non-exempt-level, benefited position. Learn more about UVA benefits. This is a restricted position, which is dependent on funding and is contingent upon funding availability. This position is based in Charlottesville, VA, and must be performed fully on-site.

About UVA and the Community

To learn more about UVA and in the Charlottesville area, visit UVA Life and Embark CVA.

Additional Requirements

Background checks, pre-employment health screenings, and drug screenings will be conducted on all new hires prior to employment.

How to Apply

Please apply online, by searching for requisition number R0080247. Complete an application with the following documents:  

Resume Cover Letter

Upload all materials into the resume submission field. You can submit multiple documents into this one field or combine them into one PDF.   Applications without all required documents will not receive full consideration.

Internal applicants: Search and apply for jobs on the UVA Internal Careers website.

Reference Check Process

Reference checks will be completed by UVA’s third-party partner, SkillSurvey, during the final phase of the interview. Five references will be requested, with at least three responses required. 

Contact

For questions about the application process, please contact Jeremy Brofft, Senior Academic Recruiter at xmf9ad@virginia.edu.

The University of Virginia is an equal opportunity employer. All interested persons are encouraged to apply, including veterans and individuals with disabilities. Learn more about UVA’s commitment to non-discrimination and equal opportunity employment.