Site Contract Specialist I - Clinical Trials (Canada)

Psi CRO; Canada; On-site; CAD 65,000 - 95,000; Full time

Job summary

PSI CRO is seeking a Site Contract Specialist I who can be based anywhere in Canada. The role centers on negotiating site agreements and budgets to support site activation, tailoring agreements for country and site needs, and coordinating the signing process.

Responsibilities include tracking negotiations, maintaining Trial Master File records, and keeping stakeholders informed of contracting progress. A relevant college or university degree and clinical research experience are required, with

Qualifications

• Minimum 2 years experience in a clinical research environment.
• Experience negotiating site budgets is required.
• Knowledge of legal documents related to clinical trial sites is a plus.

Responsibilities

• Facilitate negotiations of site agreements and budgets to align with site activation plan.
• Customize and prepare country- and site-specific agreements and arrange translations.
• Track status of site agreement and budget negotiations.
• Prepare executable site agreements and budgets and coordinate signatures.
• File executed site agreements in the Trial Master File.
• Update all concerned functions on the site contracting process.

Skills

Negotiation

Budget management

Documentation

Education

College or university degree

Job description

PSI CRO is seeking a Site Contract Specialist I who can be based anywhere in Canada. The role centers on negotiating site agreements and budgets to support site activation, tailoring agreements for country and site needs, and coordinating the signing process.

Responsibilities include tracking negotiations, maintaining Trial Master File records, and keeping stakeholders informed of contracting progress. A relevant college or university degree and clinical research experience are required, with