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Clinical Trial Associate

  • Burlington, ON, Canada
  • Canada, Burlington, 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
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


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.


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


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

More about this job

Responsibilities

Coordinate and administer clinical trials, maintain study and regulatory documentation, and support the preparation of study materials. Collaborate with cross-functional teams and track and report trial metrics and milestones to support smooth trial execution.

Requirements

Requires a bachelor's degree in a scientific or healthcare-related field and at least two years of experience supporting clinical trials. Candidates should know 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
  • Regulatory Compliance
  • Clinical Trial Documentation
  • Regulatory Documentation Management
  • Informed Consent Forms
  • Case Report Forms
  • Cross-Functional Communication
  • Clinical Trial Metrics Tracking
  • Milestone Reporting
  • Organization
  • Attention to Detail
  • Team Collaboration

Benefits

  • Performance-Related Incentives
  • Medical Coverage
  • Dental Coverage
  • Vision Coverage
  • Retirement and Pension Plans
  • Life Assurance
  • Disability Coverage
  • Employee Assistance Programs
  • Wellbeing Resources
  • Learning and Development Opportunities

Visa sponsorship

Not detected in the job text

Categories

  • Healthcare
  • Science & Research
  • Administrative

Keywords

  • Clinical Research
  • Clinical Trials
  • Clinical Trial Coordination
  • Clinical Trial Administration
  • Study Files
  • Essential Documents
  • Regulatory Submissions
  • Regulatory Documentation
  • Clinical Trial Protocols
  • Regulatory Requirements
  • Clinical Trial Processes
  • Clinical Trial Regulations
  • Clinical Trial Guidelines
  • Informed Consent Forms
  • Case Report Forms
  • Cross-Functional Teams
  • Clinical Trial Metrics
  • Trial Milestones
  • Sponsor-Dedicated Model
  • Scientific Field
  • Healthcare

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