Regional Project Lead

PSI CRO AG · Toronto, Canada · full-time · Remote · August 14, 2026

Sign up to apply
Your first one is free
Posted August 14, 2026 · Read from PSI CRO
Why a CV for this job?

94% of employers say their filters drop qualified candidates whose CV does not match the ad's exact criteria (Harvard Business School, 2021).

  • They see what they asked for, first. Your experience that matches the ad leads, in the ad's own words, so someone skimming finds it in seconds.
  • It gets past the software. Many larger employers use software that ranks CVs by how closely they match the ad, often before anyone reads them.
  • In the language of the ad. An ad written in Spanish gets a CV in Spanish, even when yours is in Portuguese.
  • Your facts, nothing invented. Your own experience, reordered and reworded. What the ad wants and your CV does not show is listed for you to add, only if it is true. You check it before you send it.
See an example

Job Description

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.

The scope of responsibilities will include:

  • 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 NA.

Qualifications

  • 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.

Additional Information

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.

Employer
PSI CRO AG
Location
Toronto, Canada · Remote
Contract
full-time