We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

The Site Contract Specialist can be based anywhere in the United States.The core responsibilities of this role include: Facilitatingnegotiations of site agreements and budgets to ensure alignment with the site activation plan Customizingand preparingcountry- and site-specific agreements and organizing their translations Trackingthe status of site agreement and budget negotiation Preparingexecutable versions of site agreements and budgets, and coordinatingthe signature process Filingexecuted site agreements in the Trial Master File Updatingall 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 2years 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. 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. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future #J-18808-Ljbffr Experience: 3 years required