Clinical Research Coordinator, Non Licensed
Job location: Charlottesville, VA
Employment Type: Full-time
Posted data: 2021-06-02
The Department of Medicine, Division of Digestive Health is seeking candidate to join a Clinical Research team. This position is open to candidates at the CRC Intermediate and CRC Senior levels. Position coordinates and implements clinical research studies conducted by investigators for the Division of Gastroenterology and Hepatology. The incumbent collaborates with Principal Investigator for patients on clinical trials; collects and analyzes clinical research data; prepares appropriate documentation; and ensures compliance with protocol guidelines and requirements of regulatory agencies. Incumbent is responsible for maintaining quality management of the trial portfolio.
To be considered for the Clinical Research Intermediate, Non-Licensed position, candidates must have a Bachelor's degree and a minimum of four years of clinical research experience. Related graduate degree may substitute for two years of experience. Certification as a Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred, with certification required within one year of certification eligibility.
To be considered for the Clinical Research Senior, Non-Licensed position, candidates must have a Bachelor's degree and a minimum of six years of clinical research experience. Related graduate degree may substitute for three years of experience. Certification as a Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is required. A Master's degree in related field with related work experience may sub at time of hire, with certification required within one year of certification eligibility.
- Recruit, screen, and enroll study participants who meet research criteria. Collect basic information through scripted interviews and answer general questions.
- Obtain informed consent from study participants and maintain telephone and in-person contact. Notify Principal Investigator and supervisor of subject status.
- Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols. Prepare documentation, reports, graphs, and other materials. Keep appropriate logs, track participants, and prepare study materials.
- Process, prepare and ship laboratory specimens.
- Compile and submit study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor or Principal Investigator.
In addition to the above job responsibilities, other duties may be assigned.
- Experienced with direct patient care is required
- Medical-clinical experience required
- IRB experience preferred
- Phlebotomy and shipping of specimens experience preferred
- Knowledge and past experience with FDA studies and regulations preferred
To apply please visit UVA job board https://uva.wd1.myworkdayjobs.com/UVAJobs, and search for "R0024985". Complete the application and see below for documents to attach. Please note that multiple documents can be uploaded in the CV/Resume box.
Required Application Materials:
- Cover Letter
- Contact information for 3 references
The selected candidate will be required to complete a background check at time of offer per University Policy.
The University of Virginia, including the UVA Health System which represents the UVA Medical Center, Schools of Medicine and Nursing, UVA Physician’s Group and the Claude Moore Health Sciences Library, are fundamentally committed to the diversity of our faculty and staff. We believe diversity is excellence expressing itself through every person's perspectives and lived experiences. We are equal opportunity and affirmative action employers. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender identity or expression, marital status, national or ethnic origin, political affiliation, race, religion, sex (including pregnancy), sexual orientation, veteran status, and family medical or genetic information.