About the Role

Our client is a global biopharmaceutical company with a broad portfolio of vaccines and medicines. They are looking for a Clinical Study Manager to run the Canadian operations for global clinical trials. You'll work with global study teams, local cross-functional partners and investigator sites to deliver studies on time, on budget and to a high standard of quality.

This role suits someone who communicates clearly, makes practical decisions, builds trust easily and enjoys developing others. It's a visible leadership role with strong room for career growth.

What You'll Do

Lead the local study team and coordinate cross-functional contributors on your assigned Canadian studies.
Run local start-up from beginning to end: feasibility, site selection, regulatory and ethics submissions, and site activation.
Plan and execute site activation so studies meet their enrollment targets and timelines.
Manage timelines, budgets and resources. Spot risks early and put mitigation plans in place to keep studies on track.
Track study progress against agreed metrics, and lead corrective action when performance falls short.
Manage study-level finances and contribute to site contract and budget negotiations.
Oversee CRO and vendor performance so it supports study objectives and meets local requirements.
Keep trial documentation complete and inspection-ready, and support data integrity and GCP compliance.
Make sure studies follow ICH-GCP, Canadian regulations and internal standards.
Serve as the main operational link between the global study team and Canadian sites.
Give global and local stakeholders clear updates on study status, risks and decisions.
Coach and support local study staff, sharing practical improvements and building the team's capabilities.

Minimum Qualifications

Bachelor's degree in life sciences, nursing, pharmacy, clinical research or a related field, or equivalent experience
3+ years in clinical research or clinical study operations
Project management experience, including oversight of timelines and budgets
Hands-on experience across the study lifecycle: start-up, recruitment and close-out
Strong stakeholder management and cross-functional collaboration skills
Excellent written and spoken English

Preferred Qualifications

Advanced degree in life sciences, clinical research or a related discipline
Experience leading multi-site or multi-country studies alongside global central teams
Experience managing CROs and vendors, including vendor oversight plans
Working knowledge of Health Canada processes and local ethics submission requirements
Familiarity with eTMF, CTMS or other clinical operations systems
Experience supporting audits, inspections or CAPA plans

Working Model

This is a hybrid role based in the Greater Toronto Area. You'll be in the office 2–3 days per week. Fully remote arrangements are not available.

Compensation

The salary range for this role is CAD $117,000–$167,000. Where you land in the range depends on your experience, qualifications and internal equity.

Interested?

We'd love to hear from people who bring scientific curiosity, a collaborative approach and a focus on patients. If this sounds like you, please apply.