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Clinical Research Associate Jobs

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  • DOCS - ICON Resourcing Solutions
  • Oakland, California 94612 United States
  • 05/10/2012
  • Monitoring
The Role and your Responsibilities CRA II for long term contracts. Assist in managing clinical studies Plan, implement, motivate, co-monitor, manage, and track clinical trials Assist in the supervision of field monitors, CROs Establish effective relationships with...  More Details
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  • Research CRA II Salary Research Salary
  • Analgesic Solutions LLC
  • Natick, Massachusetts 01760 United States
  • 05/08/2012
  • Clinical Operations
Analgesic Solutions, an international leader in the area of pain research and the development of analgesics, is looking for a talented Clinical Research Associate to be an integral part of our dynamic clinical team. ...  More Details
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  • Research Clinical Research Associate – Clinical Trials Management (CTM) Salary Research Salary
  • DOCS - ICON Resource Solutions
  • Oakland, California 94612 United States
  • 05/10/2012
  • Monitoring
In-house Contract Sr. CRA opportunity The Role and your Responsibilities Assist in managing clinical studies Plan, implement, motivate, co-monitor, manage and track clinical trials Assist in the supervision of field monitors,...  More Details
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  • Research In-house CRA Salary Research Salary
  • Paragon Biomedical, Inc
  • Unspecified, Colorado United States
  • 05/01/2012
  • Monitoring
Company Info: Paragon Biomedical specializes in customized, international Phase I-IV clinical trials management. With offices in the US, UK and India, we deliver expertise, services, and resources through clinical and biometrics management teams experienced in local customs, culture, language, and regulations....  More Details
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  • Research CRA/Clinical Research Associates-Home Based Salary Research Salary
  • PPD, Inc.
  • Unspecified United States
  • 04/27/2012
  • Clinical Operations
North East region includes: CT, DE, KY, MA, ME, MD, NC, NH, NJ, NY, OH, PA, RI, TN, VT, VA, WV   The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures.  ...  More Details
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