Trial Delivery Manager (TDM) - Home Based - Canada

ICON Strategic Solutions; Canada; Remote; CAD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a Trial Delivery Manager to lead clinical trials from start to finish. This remote role offers the chance to work with a global team, ensuring compliance with health regulations while managing budgets and vendor relationships. If you have a background in Life Sciences and experience in clinical trial management, this is an exciting opportunity to contribute to innovative healthcare solutions. Join a diverse and high-performing team that values talent development and offers comprehensive benefits, including health insurance and retirement plans.

Benefits

Health insurance options

Retirement plans

Global Employee Assistance Programme

Life assurance

Gym memberships

Childcare vouchers

Various annual leave entitlements

Qualifications

• 3-5 years of clinical trial management experience in the pharmaceutical industry.
• Experience managing trials from Start-Up to Database Lock and Trial Closure.

Responsibilities

• Oversee the setup, planning, and coordination of clinical trials.
• Manage budgets and coordinate third-party vendors.

Skills

Clinical Trial Management

Vendor Management

Team Leadership

Budget Management

Education

BS degree in Life Sciences

Job description

Trial Delivery Manager (TDM) - Home Based - Canada

Join to apply for the Trial Delivery Manager (TDM) - Home Based - Canada role at ICON Strategic Solutions.

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

What will you be doing?

Joining a well-established yet expanding team fully outsourced to one of our global pharmaceutical clients, the Clinical Trial Manager ensures the successful execution of phase 1-4 clinical trials across multiple therapeutic areas, in accordance with SOPs, timelines, budgets, and regulatory requirements on a global scale.

The Clinical Trial Manager leads the Study Management Team, overseeing the setup, planning, and coordination of clinical trials through to closure. Managing study metrics, communicating across departments, and ensuring adherence to milestones are key responsibilities.

Reporting to a Clinical Program Leader, you will manage budgets, coordinate third-party vendors, and ensure compliance with health authority regulations and SOPs. Participation in audits and inspections may be required.

You will provide training to study teams, liaise with Quality Management, and ensure high-quality standards throughout the project lifecycle.

The ideal candidate is an experienced study manager with a proven record of managing global clinical trials, capable of motivating virtual teams, and experienced in vendor management and study startup processes, preferably with Phase I-IV studies.

Minimum Requirements

• BS degree or equivalent, preferably in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
• 3-5 years of clinical trial management experience in the pharmaceutical industry or CRO
• Experience managing trials from Start-Up to Database Lock and Trial Closure
• Experience coordinating global or regional virtual teams for at least 3 years
• Willing to travel up to 20%
• Legally authorized to work in the US and/or Canada; sponsorship not required

Position is remote from home.

What ICON Can Offer You

We prioritize diversity, high performance, and talent development. Our benefits include:

• Various annual leave entitlements
• Health insurance options
• Retirement plans
• Global Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym memberships, and more

Visit our benefits webpage for more information.

ICON values inclusion and provides an accessible environment for all candidates. We are committed to equal opportunity employment.

Interested but unsure if you meet all requirements? We encourage you to apply anyway.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Industry: Pharmaceutical Manufacturing