The Site Contract Specialist can be based anywhere in the United States.
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 sitespecific 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.
Additional Information :
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.
Remote Work :
Yes
Employment Type :
Fulltime