Regional Project Lead

PSI CRO AG

Regional Project Lead coordinating clinical trial operations across North America for PSI, a global pharmaceutical CRO. Overseeing sites, milestones, training, payments, and audits.

Posted 8/7/2026full-timeRemote • 🇨🇦 CanadaSenior💰 CA$140,000 - CA$155,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Operations management, ensuring compliance with project timelines, subject enrollment targets, and training standards. Proficient in overseeing project teams, site selection, and monitoring activities within the clinical research domain.

Highest-signal resume keywords

Clinical Project ManagementSite Monitoring ExperienceLead Monitor ExperienceOncology ExperienceMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsProject PlanningStudy MonitoringBudget NegotiationContractual NegotiationField TrainingCompliance ManagementStudy Audit PreparationProject Status ReportingSubject Enrollment Management

Soft Skills

Communication SkillsPresentation SkillsCustomer-Service SkillsTeam BuildingLeadership SkillsOrganizational Skills

Tools & Technologies

MS OfficeMS Project

Certifications & Qualifications

MPharmRN

Industry Keywords

Life SciencesOncologyGastroenterologyInfectious DiseasesAutoimmune DiseasesRare Diseases

About the role

Key responsibilities & impact

Streamline activities of project teams and ensure consistency of Clinical Operations processes across North America
Ensure study milestones are met by project teams at country level
Report study progress to clients and global stakeholders
Act as project management contact for project teams and PSI support services
Review study status and progress; collect and report project status updates
Develop and update project planning documents, essential study documents, and project manuals/instructions
Ensure project timelines and subject enrollment targets are met
Coordinate study-specific and corporate tracking systems
Oversee site selection and startup, contractual negotiations, and budget negotiations
Supervise project team and site training; perform field training of monitors
Ensure compliance with project-specific training matrices
Supervise site selection, initiation, monitoring, and closeout visits
Review site visit reports and ensure monitoring and reporting standards are met
Oversee investigator and site payments
Supervise preparation for study audits/inspections and resolution of findings
Participate in regional project oversight for North America

Requirements

What you’ll need

MPharm, RN, or university/college degree in Life Sciences, or equivalent combination of education, training, and experience
Minimum 4 years of site monitoring experience
At least 2 years of experience as Lead Monitor
Experience supervising clinical project activities and leading clinical project teams
Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or rare disease indications preferred
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

Benefits

Comp & perks

Stable and secure workplace
Inclusive culture
Professional development and success investment
Remote work option