Monday, December 26, 2011
Clinical Research Associates (CRAs) and Clinical Project Managers
Clinical Research Associates (CRAs) monitor the progress of clinical trials at investigative sites, and ensures that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), company business practices, ICH guidelines, and all applicable regulatory requirements. Our CRAs travel 50-70% and must have prior monitoring experience. We are looking for both regionally-based CRAs and for those able to work out of our Durham, NC headquarters. You must have prior experience as a monitor.
Clinical Project Managers lead clinical studies and cross-departmental project teams to ensure that projects are completed in accordance with contract and client expectations. The Project Managers schedule, supervise, and deliver services to clients to fulfill contract in accordance with client needs, FDA regulations, ICH guidelines and HD SOPSs as well as manage project and project timelines through all project phases, from startup through closeout. Project Managers must be able to work out of their Durham, NC headquarters.
In-House CRAs support clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, ICH guidelines and all applicable regulatory requirements. They also serve as the remote site contact and central IRB contact, maintain study applications including the study portal and trial management system, review essential documents for content through all phases of the study and maintain study central files and site regulatory files. The In House CRAs must be able to work from of the Durham, NC headquarters.
For more information, visit http://www.healthdec.com/. To apply, submit your resume to firstname.lastname@example.org.
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