Clinical Trial Manager

PRA HEALTH SCIENCES; Canada; Remote; CAD 80,000 - 110,000; Full time

Job summary

Join the largest clinical research organization as a Clinical Trial Manager. You will oversee trial operations, ensure compliance with guidelines, and lead cross-functional teams. This role requires strong project management skills and at least 3 years of clinical trial experience. Join us to make a significant impact in the research field.

Benefits

Annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible, country-specific benefits

Qualifications

• At least 3 years of clinical trial experience, or 2 years with advanced degree.
• Strong knowledge of ICH/GCP guidelines and regulatory requirements.
• Experience in protocol development and trial monitoring.

Responsibilities

• Manage day-to-day operations of assigned trials.
• Oversee data cleaning, analysis, and review of results.
• Participate in vendor selection and manage trial budgets.

Skills

Project management

Leadership

Communication

Administration

Clinical trial management

Education

BA/BS or advanced 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, 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 as needed.
• Develop core trial documents, trial plans, and system setup; ensure operational excellence of protocols and systems.
• Participate in vendor selection, manage interactions, and escalate issues with trial vendors.
• Assess feasibility and select countries and sites for trial conduct.
• Engage with investigators and staff to support trial milestones.
• Oversee data cleaning, analysis, and review of results and statistical plans.
• Coordinate training for investigators and site monitors.
• Provide oversight to trial team members for deliverables.
• Manage trial budgets and vendor contracts.
• Ensure quality and completeness of TMF.
• Participate in inspection readiness activities.
• Implement patient-focused strategies where applicable.
• Manage budgets, timelines, and resources for trials.

Qualifications

Qualifications:

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

What ICON can offer you:

Our success depends on the quality of our people. We prioritize a diverse culture that rewards high performance and nurtures talent. Benefits include:

• Various annual leave entitlements.
• Health insurance options.
• Retirement planning options.
• Global Employee Assistance Programme.
• Life assurance.
• Flexible, country-specific benefits.

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

ICON values inclusion & belonging. We are committed to an inclusive, accessible environment and provide equal employment consideration. For accommodations, please contact us through the provided form: https://careers.iconplc.com/reasonable-accommodations

If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for!