Site Contract Specialist I

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

Job summary

A leading global company in the pharmaceutical industry is seeking a Site Contract Specialist based anywhere in Canada. The role involves negotiating site agreements, preparing contracts, and ensuring compliance with activation plans. Join a dynamic team dedicated to improving lives through medical science.

Qualifications

• Minimum 2 years of relevant experience required.
• 1 year experience in clinical research in the US.

Responsibilities

• Facilitating negotiations of site agreements and budgets.
• Preparing executable versions of site agreements and budgets.
• Tracking the status of site agreement negotiations.

Skills

Negotiation

Knowledge of Medical Terminology

Education

College or University Degree

Job description

Company 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:

1. Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan.
2. Customizing and preparing country- and site-specific agreements and organizing their translations.
3. Tracking the status of site agreement and budget negotiation.
4. Preparing executable versions of site agreements and budgets, and coordinating the signature process.
5. Filing executed site agreements in the Trial Master File.
6. 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.
• 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.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Research

Industries

• Pharmaceutical Manufacturing

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