Clinical Research Coordinator Intermediate, Non-Licensed

Charlottesville, VA
Feb 28, 2018
Institution Type
Four-Year Institution

Working Title: Clinical Research Coordinator Intermediate, Non-Licensed

Position Type: University Managerial and Professional Staff

Department: Department of Medicine, Cardiovascular Medicine

Location: Charlottesville

Posting Date: 02-19-2018

Posting Summary:
The Cardiovascular Division in the Department of Medicine is seeking a Clinical Research Coordinator, Intermediate, Non-Licensed. This position provides clinical trial management for new and existing research trials.

The incumbent works with the Principal Investigator, human subjects, IRB, University and the company and/or government sponsor to ensure smooth, accurate progress of clinical trials from the planning stage through trial completion and post-study closure. Duties include support of financial accountability, coordination of subject recruitment and consent, scheduling of study procedures and research visits, and collection of study data.

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

Qualified applicants must have a Bachelor's degree or higher and a minimum of four years of clinical trial research experience. Related graduate degree may substitute for two years of experience. One or more years' experience with clinical Cardiovascular Disease preferred; experience with clinical electrophysiology is strongly preferred. Certification as a Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred and is required within one year of eligibility. Candidate must have strong knowledge of Microsoft Office (Word, Excel, PowerPoint, and Outlook). Working knowledge of UVA patient scheduling and electronic medical records system is preferred.

Required Knowledge, Skills and Abilities:
1. Knowledge of human subject research ethics.
2. Intermediate knowledge of IRB procedures and submission process along with the federal regulations of working with human subjects.
3. Demonstrated ability to perform technical, analytical, and professional level work.
4. Considerable knowledge of scientific principles and research methodology.
5. Proficient knowledge of medical terminology associated with diseases/conditions under study and Good Clinical Practices for research.
6. Ability to identify and resolve problems.
7. Ability to work accurately and with attention to detail.
8. Proficient keyboarding skills.
9. Ability to sort and compile data.
10. Strong organizational skills with the ability to manage large volumes of information.
11. Flexibility and ability to adjust to changing priorities.
12. Ability to work independently.
13. Ability to learn new information under supervision of others.
14. Ability to work with diverse community of people.
15. Ability to relate to people in a wide variety of professional levels.
16. Excellent interpersonal, written and organizational communication skills.
17. Detail oriented with excellent analytical skills
18. Demonstrated ability to learn the organization, policies and procedures associated with clinical research.
19. Ability to maintain confidentiality.

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