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Clinical Research Associate

Location:Cariboo, British Columbia, Canada
Job Type:Contract
Posted:11th Sep 2009
Closing Date:9th Oct 2009
Posted By:Biorole
Details:
Clinical Research Associate

Clinical Research Associate

GENERAL DUTIES/RESPONSIBILITIES

Conducts investigational site selection, initiation, periodic and termination visits. Serves as liaison between
the sponsor and the investigator, and participates in project team meetings and sponsor telephone conference calls on a regular basis.

Other responsibilities include verifying proper storage conditions, accountability, and disposition of the investigational products; maintenance of up-to-date and accurate investigator study files; and accurate recording and reporting of adverse events. Writes and submits written reports of investigational site findings. May be involved in organizing or participating in Investigator's Meetings, study report writing, and the development of Protocols, Case Report Forms and Study Procedures Manuals.

Maintains a high level of professional expertise through familiarity with regulatory and clinical literature and continuous education.

REQUIRED EXPERIENCE

BSc in a life sciences field or be a registered nurse
Ability to travel up to60% required
Good Computer skills
Excellent Written and Oral Communication Skills
Work experience or a certificate with ICH GCP
 
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