Depending on experience responsibilities include:
* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
* All aspects of site and registry management as prescribed in the project plans
* Organize and make presentations at Investigator Meetings
* Report, write narratives and follow-up on serious adverse events ...
Clinical Research Advantage, Inc. (CRA) has provided research services to the pharmaceutical industry for over 20 years. With CRA, Pharmaceutical, Biotech, and CRO companies have a unique source for conducting clinical drug trials. CRA is comprised of community based Investigators plus an experienced staff of Clinical Research Coordinators. The key to our success has been the development of research departments within established family, internal medicine, pediatrics and neurology practices. Our ...
Radiant Research Inc. (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research ...
Oct 22 -
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