Compensation: CAD 140000 - CAD 155000 - yearly PSI is a leading Contract Research Organization (CRO) with over 30 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

We are not just about conducting clinical trials; we are about building a community where every team member has the chance to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.

Act as project management contact for the project team and PSI support services. Perform study status review and progress reporting, collect and report project status updates. Develop and update project planning documents, essential study documents and project manuals/ instructions.

Ensure that the project timelines and subject enrollment targets are met.



Coordinate maintenance of study-specific and corporate tracking systems. Oversee site selection and startup, site contractual and budget negotiations.

Supervise project team and site training, perform field training of monitors tailored to the project needs. Ensure team compliance with project-specific training matrix. Supervise preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits.

Review site visit reports and ensures monitoring and reporting standards are met. Oversee investigator and site payments. Supervise project team preparation for study audits/ inspections and resolution of audit/ inspection findings.

Might be involved in regional project oversight for APAC. MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience. Minimum 4 years’ site monitoring experience and at least 2 years’ experience as Lead Monitor.

Experience supervising clinical project activities and leading clinical project teams.

Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable. Communication, presentation, and customer-service skills. Team building, leadership and organizational skills. Full working proficiency in English. Proficiency in MS Office applications, including MS Project.

📌 Clinical Regional Project Lead (Toronto)
🏢 PSI CRO
📍 Toronto