Clinical Research Coordinator - Cardiovascular

RPS is looking for clinical research coordinators (CRC) for sites in Detroit MI & Chicago IL. These are full-time, temporary assignments, expected to last through the end of patient enrollment. Some regional domestic travel may be required. The current target date to complete enrollment is December 31, 2008.


RESPONSIBILITIES



·  Collaborate with team members to ensure clinical trial success

·  Maintain all clinical trial documentation and data

·  Assist in patient identification

·  Perform Informed Consent

·  Complete Case Report Forms (CRF)

·  Follow-up with patients


QUALIFICATIONS

Minimum 3 years experience as a clinical research coordinator is required. RN or LPN preferred. CCRP preferred. Previous experience in high-enrollment clinical research trials is preferred. Previous experience in cardiovascular clinical trials is preferred. Excellent verbal & written communication skills required. Excellent time-management and organizational skills is required. Experience with MS Office suite required.


ABOUT RPS

 

ReSearch Pharmaceutical Services Inc (RPS) is the market leader in providing integrated global clinical development solutions to the pharmaceutical industry, based on its comprehensive therapeutic expertise, robust clinical operations infrastructure, and highly- trained and experienced employees. RPS is the industry's first Pharmaceutical Resource Organization (PRO), built to offer unique, integrated, and global solutions to the Pharmaceutical, Biotechnology and Medical Device industries. By combining an experienced clinical research operations infrastructure with the industry's largest resourcing engines, RPS is able to provide its clients with the highest-quality services through innovative, cost-effective, integrated functional clinical development solutions, that speed the development of new life-changing therapeutics. Learn more about RPS at www.rpsweb.com