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Clinical Trial Associate

  • Burlington, ON, Canada

Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience · Full-time

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience
Job type
Full-time
Closing date
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

Clinical Trial Associate (Hybrid role in Mississauga)

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 Do

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key Responsibilities Include

  • 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

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required Qualifications And Experience

  • Bachelor's degree in a scientific or healthcare-related field.
  • A minimum of two years of experience supporting clinical trials
  • Knowledge of clinical trial processes, regulations, and guidelines.
  • Excellent organizational and communication skills.
  • Ability to work collaboratively in a fast-paced environment with attention to detail.
  • Experience managing regulatory documentation for clinical trials
  • Willingness to report to the Mississauga office 3 days per week

Pay Range ($55,000 – $67,000 CAD) - Actual salary will be based on experience

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply
More about this job

Responsibilities

Coordinate and administer clinical trials while maintaining study files, essential documents, and regulatory submissions in compliance with protocols and requirements. Prepare study materials, collaborate with cross-functional teams, and track and report trial metrics and milestones.

Requirements

A bachelor's degree in a scientific or healthcare-related field and at least two years of experience supporting clinical trials are required. Candidates should understand clinical trial processes, regulations, and guidelines, have experience managing regulatory documentation, and demonstrate strong organizational, communication, collaboration, and attention-to-detail skills.

Skills

  • Clinical Trial Coordination
  • Clinical Trial Administration
  • Clinical Trial Documentation
  • Regulatory Documentation
  • Regulatory Compliance
  • Clinical Trial Processes
  • Clinical Research
  • Informed Consent Forms
  • Case Report Forms
  • Cross-Functional Communication
  • Clinical Trial Metrics Tracking
  • Milestone Reporting
  • Organization
  • Communication
  • Attention to Detail
  • Team Collaboration

Benefits

  • Annual Leave
  • Health Insurance
  • Retirement Planning
  • Employee Assistance Programme
  • Life Assurance
  • Childcare Vouchers
  • Bike Purchase Schemes
  • Discounted Gym Memberships
  • Subsidized Travel Passes
  • Health Assessments

Visa sponsorship

Not detected in the job text

Categories

  • Healthcare
  • Science & Research
  • Administrative

Keywords

  • Clinical Trials
  • Clinical Research
  • Clinical Trial Coordination
  • Clinical Trial Administration
  • Study Files
  • Essential Documents
  • Regulatory Submissions
  • Regulatory Documentation
  • Regulatory Requirements
  • Clinical Trial Protocols
  • Informed Consent Forms
  • Case Report Forms
  • Trial Metrics
  • Trial Milestones
  • Cross-Functional Teams
  • Pharmaceutical Manufacturing
  • Sponsor-Dedicated Model

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