Clinical Trial Manager - Canada Remote

PRA HEALTH SCIENCES; Canada; Remote; CAD 80,000 - 120,000; Full time

Job summary

A leading healthcare organization seeks a Clinical Trial Manager to oversee the day-to-day operations of clinical trials, ensuring compliance with GCP/ICH guidelines. The role requires strong project management skills and a solid understanding of trial design and monitoring, as well as excellent communication abilities. The successful candidate will participate in vendor management and budget oversight while fostering a culture of inclusion and supporting trial milestones.

Benefits

Annual leave entitlements

Health insurance options

Retirement planning

Global Employee Assistance Programme

Life assurance

Optional benefits like childcare vouchers

Qualifications

• At least 3 years of clinical trial experience or 2 years with advanced degree.
• Knowledge of protocol development, trial design, and monitoring.
• Willingness to travel approximately 25%.

Responsibilities

• Manage day-to-day operations of assigned trials.
• Oversee data cleaning, analysis, and statistical plans.
• Ensure quality and completeness of Trial Master File (TMF).

Skills

Project management skills

Strong knowledge of ICH/GCP guidelines

Excellent communication skills

Education

BA/BS degree

MS/PhD/PharmD

Job description

Overview

As a Clinical Trial Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

What you will be doing:

• Manage the day-to-day operations of assigned trials to ensure completion per project goals and in compliance with GCP/ICH guidelines and regulatory requirements.
• Lead or support cross-functional trial teams, including vendors.
• Maintain accurate trial information in tracking systems and provide regular updates to stakeholders.
• Identify and resolve issues during trial conduct; escalate trial-related issues when necessary.
• Develop core trial documents, trial plans, and system setup; ensure operational excellence of protocols and systems.
• Participate in vendor requirements, project scope, and vendor management.
• Assist in feasibility assessments and site selection for trials.
• Engage and communicate with investigators and staff to support trial milestones.
• Oversee data cleaning, analysis, and topline results; review statistical analysis plans.
• Coordinate training for investigators and site monitors.
• Provide oversight to trial team members for deliverables.
• Manage trial budgets and vendor contracts, tracking in systems.
• Ensure quality and completeness of Trial Master File (TMF).
• Participate in inspection readiness activities.
• Implement patient-focused strategies for trials, as applicable.
• Manage budgets, timelines, and resources for clinical trials.

Qualifications

Qualifications:

• BA/BS degree with at least 3 years of clinical trial experience or an advanced degree (MS/PhD/PharmD) with at least 2 years of experience.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Understanding of protocol development, clinical trial design, planning, and monitoring.
• Project management skills and trial leadership ability.
• Excellent communication, administrative, and computer skills.
• Fluent in English.
• Willingness to travel approximately 25%.

What ICON can offer you:

Our success depends on our people. We prioritize building a diverse culture that rewards performance and nurtures talent. Besides a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

• Annual leave entitlements
• Health insurance options
• Retirement planning
• Global Employee Assistance Programme, TELUS Health
• Life assurance
• Optional benefits like childcare vouchers, gym discounts, travel passes, health assessments, etc.

Visit our careers site for more: https://careers.iconplc.com/benefits

ICON values inclusion and belonging, providing an accessible environment for all candidates. We are committed to equal opportunity employment. If you need accommodations during the application process, please let us know at https://careers.iconplc.com/reasonable-accommodations.

Interested but unsure if you meet all requirements? We encourage you to apply. You might be exactly what we’re looking for!