Clinical Research Coordinator Intermediate, Licensed
Working Title: Clinical Research Coordinator Intermediate, Licensed
Position Type: University Managerial and Professional Staff
Department: Department of Urology
Posting Date: 01-31-2017
The University of Virginia's Department of Urology is seeking a Clinical Research Coordinator Intermediate, Licensed. This position coordinates and implements clinical trial research studies in the Department of Urology. The incumbent collaborates with Principal Investigators 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.
Qualified applicants must have a Bachelor's degree and have a minimum of four years of clinical research experience. A related graduate degree may substitute for two years of experience. Clinical Research Coordinator (CCRC) or Clinical Research Associate (CCRA) certification is preferred and required within one year of eligibility.
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 the ability to keep detailed records and to manage and analyze confidential data. Knowledge of sponsored clinical trials; proficient knowledge of medical terminology; and knowledge of IRB procedures and submission processes along with federal regulations are required.
This position is restricted and contingent upon the continuation of funding.
Required Knowledge, Skills and Abilities:
1. Knowledge of good clinical practices.
2. Good communication and interpersonal skills.
3. Initiative to develop professionally and improve the clinical trials process.
4. Ability to interact with patients (including children), family members, physicians, and ancillary personnel in a professional manner.
6. Ability to accurately and consistently document information.
7. Ability to work as part of a collaborative team, as well as independently
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