Clinical Research Associate
Clinical Research Associate
A Clinical Research Associate is responsible for monitoring clinical sites as a part of a larger clinical trial. CRA's will initiate new sites, train clinic staff in the procedures of the project and liaise with clinical staff through the project. They will collect data from sites, and process accordingly. CRA's will be responsible to monitor Good Clinical Practice Compliance and report adverse events.
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Responsibilities
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This position will require the CRA to visit the site for 1 initiation visit, up to 12 monitoring visits and 1 close out visit. Data processing, teleconferences, and other activities will be done off site
This position has very flexible hours, work from home opportunities, and opportunities for travel. |
Qualifications
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Candidates should have:
BSc in a life sciences field or be a registered nurse
Knowledge of Good Clinical Practices
Good Computer skills
Experience with Electronic Data Capture
Excellent Written and Oral Communication Skills
www.espoirbridge.com |
Additional Job Information
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