Site Contract Specialist I at PSI CRO

The Site Contract Specialist 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 1 year experience in the clinical research industry in the United States
• Previous experience with negotiating site budgets
• Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.