Clinical Trial Manager Salary in Canada
Clinical Trial Manager Salary Range
$108,450
$147,075
Low Range
High Range
Midpoint
This salary range represents a national benchmark in CAD. Regional salary adjustment factors can be applied below to estimate how compensation may shift by province or territory.
Salary benchmarks are based on a mix of TQR internal data and external market research for specialized manufacturing and technical roles in Canada.
Clinical Trial Manager salaries in the Life Sciences industry typically range from $108,450 to $147,075, with a midpoint of approximately $129,205. Compensation varies based on clinical operations experience, therapeutic area expertise, global study management, regulatory knowledge, leadership responsibilities, project complexity, and overall accountability for clinical trial execution.
What the Salary Percentiles Mean
The following range has been generated based on real salary data across North America.
$108,450
$147,075
$108,450
25th percentile
Employees in this section often have a lower level of experience or skills and
are still growing into their role. This role may also be at a small to medium-sized business.
$129,205
50th percentile
Employees in this section typically demonstrate the required level of experience plus many skills that are deemed an asset. This role is likely at a medium-sized business.
$147,075
75th percentile
Employees in this section typically demonstrate a higher-level of expertise and/or enhanced qualifications. They should also have a proven track record and cultural fit. This role is likely at a larger business.
Regional Salary Adjustments
Salary ranges can vary by region based on cost of living, labor competition, industry concentration, and talent availability. The map below shows regional adjustment factors that can be applied to the national salary benchmark as a directional guide.
Factors That Affect a Clinical Trial Manager's Salary
Clinical Trial Manager compensation can vary based on therapeutic area expertise, study complexity, clinical development phase, global trial experience, regulatory knowledge, CRO management responsibilities, leadership scope, geographic region, and overall accountability for clinical program execution. Employers may need to adjust compensation when the position manages multinational clinical trials, high-risk therapeutic programs, multiple study teams, complex regulatory submissions, or large clinical development portfolios.
Clinical Trial Manager Job Description:
A Clinical Trial Manager is responsible for planning, coordinating, and overseeing clinical trials that support the development of pharmaceutical, biotechnology, medical device, diagnostic, and related Life Sciences products. This role helps ensure clinical studies are conducted safely, ethically, efficiently, and in compliance with regulatory requirements while supporting successful product development and commercialization.
Clinical Trial Managers typically oversee study planning, site selection, investigator management, vendor coordination, patient enrollment, trial execution, monitoring activities, clinical documentation, budgets, timelines, and regulatory compliance. They work closely with Clinical Operations, Medical Affairs, Regulatory Affairs, Quality Assurance, Data Management, Biostatistics, Pharmacovigilance, CROs, investigators, and external partners to ensure studies meet protocol requirements and project objectives.
Clinical Trial Managers are expected to understand how clinical operations impact patient safety, data quality, regulatory approvals, product development timelines, and overall business success. Strong candidates typically combine clinical research expertise, project management skills, regulatory knowledge, communication abilities, leadership, and problem-solving capabilities while managing multiple clinical programs within highly regulated Life Sciences environments.
Common Responsibilities:
Managing clinical trials from study start-up through closeout while ensuring timelines, budgets, quality standards, and project objectives are achieved.
Coordinating clinical sites, investigators, CROs, vendors, and cross-functional teams to ensure successful study execution and regulatory compliance.
Monitoring study progress, patient enrollment, protocol compliance, data quality, safety reporting, and clinical performance metrics while implementing corrective actions as needed.
Collaborating with Clinical Operations, Regulatory Affairs, Medical Affairs, Data Management, Biostatistics, Quality Assurance, and external partners throughout the clinical trial lifecycle.
Managing clinical documentation including Trial Master Files (TMF), study reports, regulatory submissions, essential documents, and audit readiness activities.
Ensuring compliance with FDA, ICH-GCP, IRB/IEC requirements, global regulatory guidelines, company SOPs, and applicable clinical research standards.
Identifying study risks, managing budgets, supporting continuous improvement initiatives, and utilizing clinical trial management systems (CTMS) to optimize study performance, reporting, and operational efficiency.
Explore Current Openings
TQR recruits for specialized roles across industrial automation, manufacturing, packaging, food production, life sciences, and related technical markets. Current openings may include engineering, operations, maintenance, quality, supply chain, and plant leadership roles.
View current opportunities or submit your resume to be considered for future roles that match your background.
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