||Clinical Research Associate
||Centralized monitoring staff based out of the Winston-Salem, NC office. Only those located within the Winston-Salem, NC area need apply as we currently do not not support regional monitoring.
A Clinical Research Associate (CRA) is a professional whose function is to ensure that the clinical research being conducted at investigative study sites is in accordance with the sponsor's protocol, Food & Drug Administration (FDA) and International Conference on Harmonization (ICH) Guidelines, and Standard Operating Procedures (SOPs), as well as state and local regulations governing research.
The Clinical Research Associate acts as liaison between the investigative study sites and the contracting sponsor while conducting pre-study, initiation, interim, close-out, and audit visits. While in-house, the CRA is responsible for completing detailed monitoring visit reports and follow-up letters as well as fielding questions from investigative study sites. Additionally, the CRA supports the project team in the completion of data review and query resolution.
The qualified candidate will possess a Bachelor's degree in a health, science, or research-related field; possess excellent organizational, communication, and interpersonal skills; have a working knowledge of computers; and, be willing to travel nationwide 50% of the time.
Contact: Human Resources
Posted: Thursday, July 8, 2004
If you are interested in any of the positions listed and meet the qualifications, please send your resume and cover letter referencing the position to HumanResources@ctmsinc.com or by mail to the following address:
Attention: Human Resources
1241 Volunteer Parkway, Suite 950
Bristol, TN 37620 - 4659 USA
Thank you for your interest in CTMS.
CTMS is an Equal Opportunity Employer.