Clinical Trial Manager (Non Onc) - Canada Remote

Pharmaceutical Research Associates, Inc; Canada; Remote; CAD 80,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Trial Manager to oversee trial operations and compliance with regulatory standards. The role involves managing budgets, coordinating with vendors, and engaging with investigators to ensure successful trial outcomes. Candidates with a strong background in clinical trials and leadership capabilities are encouraged to apply.

Benefits

Competitive salary

Health insurance

Retirement plans

Flexible benefits

Qualifications

• At least 3 years of clinical trial experience or 2 years with an advanced degree.
• Strong knowledge of ICH/GCP guidelines.
• Willingness to travel approximately 25%.

Responsibilities

• Manage day-to-day operations of assigned trials.
• Lead cross-functional trial teams and vendors.
• Oversee data cleaning, analysis, and results reporting.

Skills

Project management skills

Communication

Administrative skills

Clinical trial design understanding

Fluency in English

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, ensuring completion in line with project goals, objectives, and regulatory requirements such as GCP/ICH guidelines.
• Lead or support cross-functional trial teams, including vendors.
• Maintain accurate trial information in relevant tracking systems and provide regular updates to stakeholders.
• Identify and resolve issues during trial conduct and escalate as needed.
• Develop core trial documents, trial plans, and system setups to ensure operational excellence.
• Participate in vendor requirements, project scope, and selection of trial vendors, managing interactions effectively.
• Assist in feasibility assessments and site/country selection for trials.
• Engage with investigators and staff to support trial milestones.
• Oversee data cleaning, analysis, and results reporting; participate in data reviews.
• Coordinate training for investigators and site monitors.
• Provide oversight to trial team members for deliverables.
• Manage trial budgets and vendor contracts, tracking expenses and data.
• Ensure quality and completeness of TMF documentation.
• Participate in inspection readiness activities.
• Implement patient-focused strategies where applicable.
• Manage budgets, timelines, and resources for trial responsibilities.

Qualifications

Qualifications:

• BA/BS 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 clinical trial design, planning, and management.
• Project management skills and trial leadership capability.
• Excellent communication, administrative, and computer skills.
• Fluent in English.
• Willingness to travel approximately 25%.

What ICON can offer you: We prioritize building a diverse culture that rewards high performance and nurtures talent. Benefits include competitive salary, health insurance, retirement plans, flexible benefits, and more. Visit our careers website for details: https://careers.iconplc.com/benefits

ICON is committed to inclusion & belonging, providing an accessible environment for all candidates. We welcome applications regardless of background and offer reasonable accommodations as needed. Learn more at https://careers.iconplc.com/reasonable-accommodations. We encourage you to apply even if you’re unsure about meeting all requirements.