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Clinical Research Associate

Location:central, Central Toronto, Toronto, Ontario, Canada
Job Type:Permanent
Posted:11th Dec 2007
Closing Date:29th Apr 2008
Posted By:Shared Vision Management Search
Details:
Clinical Research Associate

CRA I Responsibilities: On-site monitoring, protocol/CRF development, investigator recruitment, in-house review of clinical data, generation of project-management reports, and assisting in the preparation of clinical study reports. Travel will average 50%.

CRA I Requirements:
BS/BA/RN, minimum of 6 months monitoring experience.
Please note - We can consider RNs without a 4-year degree for CRA I/II level only.



CRA II Responsibilities:
On-site monitoring, protocol/CRF development, investigator recruitment, in-house review of clinical data, generation of project-management reports, and assisting in the preparation of clinical study reports. Travel will average 50%.

CRA II Requirements: BS/BA/RN, 2 years of related industry experience including 18+ months of experience as a field monitoring in clinical trials.
Alternatively, 12+ months of experience in field monitoring of clinical trials, plus at least one of the following qualifications:
1. 12 months of prior experience as a clinical study coordinator
2. Relevant post-graduate doctoral degree (e.g., PharmD, PhD, MD)
3. Five years of relevant work experience as a nurse or pharmacist.
 
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 This job is no longer active as the closing date for applications has passed.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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