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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 | |
| Sorry! This job is no longer active as the closing date for applications has passed. You can view other vacancies from this company (if they have any) by clicking on their name above, alternatively we may have some suggestions for similar vacancies listed below that might be of interest. | |
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