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 setting where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

The role:

Independent, proactive work to set up and monitor studies, complete reports and maintain documentation

Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions

Taking responsibility for study cost efficiency

Preparation and review of study documentation and feasibility studies for new proposals

Potential to assist in training and mentoring fellow CRAs

You will need:

18 months+ of monitoring experience in phase I-III trials as a CRA

Previous monitoring experience in medium-sized studies, including study start-up and close-out





Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data

Ability to work to tight deadlines

Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license

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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📌 Senior Clinical Research Associate (Toronto - Dermatology) (Winnipeg)
🏢 ICON Strategic Solutions
📍 Winnipeg