At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What you will be doing

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

Support the preparation of study-related materials, such as informed consent forms and case report forms.

Work with cross-functional teams to facilitate communication and ensure smooth trial execution.

Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your profile

Bachelor's degree in a scientific or healthcare-related field.

Two years experience in Clinical Research or an appropriate mix of educational/professional experience

Must have a strong understanding of regulatory documentation

Knowledge of clinical trial processes, regulations, and guidelines.

Excellent organizational and communication skills.

Prior experience or robust interest in clinical research.





Oncology experience required

Must be comfortable with a hybrid role (office/home) in Mississauga Canada

Ability to work collaboratively in a fast-paced environment with attention to detail.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives

Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

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📌 Oncology Study Delivery Associate (Hybrid - Mississauga) (Ontario)
🏢 ICON Strategic Solutions
📍 Ontario