Live opening · Posted 21 hours ago
At a glance
The key details from the original listing.
About the role
Description supplied by the original job listing.
Official job title will be Site Contract Specialist I and can be based anywhere in Canada.
The core responsibilities of this role include:
Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan
Customizing and preparing country- and site-specific agreements and organizing their translations
Tracking the status of site agreement and budget negotiation
Preparing executable versions of site agreements and budgets, and coordinating the signature process
Filing executed site agreements in the Trial Master File
Updating all concerned functions on the site contracting process
College or university degree or an equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities. Equivalency is defined as a minimum of 2 years’ experience in an environment, where relevant experience has been gained.
Minimum 2 years experience in the clinical research industry
Previous experience with negotiating site budgets
Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus.
Employment type
Full-time
Work arrangement
Yes
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