PC

PSI CRO

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PSI CRO AG is a global, full-service Contract Research Organization renowned for its reliable patient enrollment and on-time project delivery across diverse therapeutic areas.

Zug

Pharmaceutical Manufacturing
1,001–5,000 people

About

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

Open positions

Senior Clinical Research Associate

On-site · Vancouver

Conduct and report onsite monitoring visits, review case report forms, verify source documents, resolve queries, and manage communication with clinical sites. Coordinate with internal teams and vendors, support feasibility research and regulatory submissions, and participate in audits and inspections.

Project Finance Manager (Clinical Trial Proposals)

Hybrid · Mississauga

The Project Finance Manager is responsible for managing clinical project budgets, including preparation, negotiation, and ongoing maintenance. They will also handle sponsor contract development and ensure accurate reconciliation of project costs within internal systems.

Lead Clinical Research Associate

On-site · Toronto

Coordinates site feasibility, startup, and monitoring activities while managing project timelines and patient enrollment. Acts as the primary communication link between monitors, project leads, and trial sites to ensure data integrity and regulatory compliance.

Lead Clinical Research Associate

On-site · Toronto

The Lead Clinical Research Associate coordinates site feasibility, study startup, and monitors project timelines while ensuring data integrity and compliance. They also manage project teams, oversee site monitoring visits, and act as the primary communication link between various stakeholders.