Full-Time Site Contract Specialist I

The Site Contract Specialist can be based anywhere in the United States.

Core Responsibilities:

• 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

Qualifications:

• 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
• Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus

What is the last date for applying to the job?

Which countries are accepted for this remote job?