psicro

Regional Project Lead

At a Glance

Location
Toronto, Ontario, Canada
Employment
Full-time
Experience
4+ years
Posted
2026-08-14T19:10:38.038Z

Key Requirements

Required Skills

Microsoft Office

Domain Knowledge

  • Clinical
  • Education

Requirements

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.

Compensation & Benefits

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Responsibilities

In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across North America.

You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.

Perform study status review and progress reporting, collect and report project status updates.

Coordinate maintenance of study-specific and corporate tracking systems.

Oversee site selection and startup, site contractual and budget negotiations.

Supervise preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits.

About the Company

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.

In an industry where cost-cutting and layoffs are common, PSI stands out as a stable and secure workplace. Our dedication to stability is evident in our exceptionally high repeat and referral business rate and minimal staff turnover. More than 25% of our colleagues have been with us for over 10 years, contributing to our long-standing traditions and history.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.