Senior Clinical Research Associate (Toronto - Dermatology)

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. 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 Balancing sponsor generated queries 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 College degree in medicine, science, or equivalent 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. Rewards & Benefits 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. Are you a current ICON Employee? Please click here to apply.

The role involves identifying, initiating, and closing out investigational sites for phase II-IV clinical studies while ensuring adherence to ICH-GCP regulations. Responsibilities include monitoring studies, preparing regulatory submissions, and managing study cost efficiency.

Candidates need a college degree in medicine or science and at least 18 months of monitoring experience in phase I-III trials. A valid driving license and the ability to travel at least 60% of the time are required.

• Competitive Base Salary • Performance Related Incentives • Medical Coverage • Dental Coverage • Vision Coverage • Retirement And Pension Plans • Life Assurance • Disability Coverage • Employee Assistance Programmes • Wellbeing Resources • Learning And Development Opportunities

Identified from the job description. Confirm important requirements above.

• Clinical Monitoring
• ICH-GCP
• Study Start-up
• Study Close-out
• Regulatory Submissions
• Medical Data Review
• Site Management
• Feasibility Studies
• Protocol Submission
• Ethics/IRB Approval

• Healthcare
• Science & Research
• Manufacturing

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Apply by

Sep 24, 2026

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level

Application method

Direct apply is available