Clinical Research Coordinator Intermediate or Clinical Research Coordinator Intermediate, RN

Location
Charlottesville, VA
Posted
May 06, 2017
Institution Type
Four-Year Institution

Working Title: Clinical Research Coordinator Intermediate or Clinical Research Coordinator Intermediate, RN

Position Type: University Managerial and Professional Staff

Department: Department of Pediatrics

Location: Charlottesville

Posting Date: 02-04-2016

Posting Summary:
The University of Virginia's of Department of Pediatrics is seeking a Clinical Research Coordinator Intermediate or Clinical Research Coordinator Intermediate, RN. This position coordinates and implements clinical trial research studies in the Division of Pediatric Infectious Diseases. The incumbent collaborates with a Principal Investigator and nurse research coordinators 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 CRC Intermediate: Qualified applicants must have an Bachelor's degree or higher, and have a minimum of 2-4 years of clinical research experience. Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRA) certification is preferred.

To be considered for the CRC Intermediate, RN: Qualified applicants must have an Associate's degree or higher, hold a current Virginia RN license, and have a minimum of 2-4 years of clinical research experience. Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRA) certification is preferred.

Qualified applicants must possess excellent interpersonal and customer service skills with the ability to communicate effectively, both in writing and verbally, as well as have the ability to plan and execute tasks; the ability to clearly articulate specific information in the area of subject matter expertise; the ability to recruit and screen potential research participants; the ability to work independently and as part of a team; and have the ability to keep detailed records and manage and analyze confidential data. Basic knowledge of sponsored clinical trials; proficient knowledge of medical terminology; and knowledge of IRB procedures and submission processes along with federal regulations are required. Knowledge of UVa financial policies and procedures, and database development is preferred.

This position is restricted and contingent upon the continuation of funding.

Required Knowledge, Skills and Abilities:
1. Ability to work with human subjects, specifically those with diabetes.
2. Superior organizational skills.
3. Ability to communicate effectively.
4. Working knowledge of the theory, ethics, and application of the biological sciences and instrumentation related to field of assignment.
5. Ability to independently plan and execute tasks.
6. Extensive management skills of clinical research protocols
7. Ability to train and supervise and lead others.
8. Ability to work with diverse international populations.
9. Expertise of research protocols and compliance regulations for the Institutional Review Board (IRB), FDA, and NIH.

E-mail a Friend: jobs.virginia.edu/applicants/Central?quickFind=78002

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