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Canada: Sr. Clinical Research Associate

Date: 29-Jun-2016
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You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. Approximately 65% travel overall can be expected, primarily regional but will include national as needed.

Successful candidates will possess:

Bachelor's degree in a life science or related discipline OR RN/LPN with 4 years related experience.

3 years of onsite monitoring experience

Experienced in oncology/immunotherapy protocols

Strong understanding of ICH GCP Compliance

Ability to travel 65-70% of the month

To apply for this position, please visit this Website.

Thank you,
BioTech FYI Center