Site Contract Specialist I

PSI CRO; Canada; Remote; CAD 60,000 - 80,000; Full time

Job summary

A global clinical research organization is seeking a Site Contract Specialist based anywhere in Canada. This role involves negotiating site agreements, preparing specific agreements, and managing the contracting process. The ideal candidate should have a college degree and at least 1 year of clinical research experience. A significant focus will be on budget negotiation skills and familiarity with legal documents related to clinical trials.

Qualifications

• Minimum 1 year experience in the clinical research industry.
• Experience in negotiating site budgets is preferred.
• Knowledge of legal documents related to clinical trial sites is a plus.

Responsibilities

• Facilitate negotiations of site agreements and budgets.
• Prepare country- and site-specific agreements.
• Track status of site agreement and budget negotiation.
• Coordinate the signature process for agreements.
• File executed agreements in the Trial Master File.

Skills

Negotiation skills

Knowledge of clinical trial procedures

Attention to detail

Education

College or university degree or equivalent

Job description

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 2700 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 Canada.

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 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.

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.