Closed listing
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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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
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
The Clinical Trial Associate assists in the coordination and administration of clinical trials while ensuring compliance with regulatory requirements. They are responsible for maintaining study documentation and facilitating communication across cross-functional teams to ensure smooth trial execution.
Requirements
Candidates must hold a Bachelor's degree in a scientific or healthcare-related field and possess at least two years of experience in clinical trials. Proficiency in clinical trial processes, regulations, and documentation management is required.
Skills
- Clinical trial coordination
- Regulatory compliance
- Documentation management
- Study file maintenance
- Regulatory submissions
- Informed consent forms
- Case report forms
- Cross-functional collaboration
- Clinical trial metrics
- Clinical research
- Communication skills
- Organizational skills
- Attention to detail
Benefits
- Medical coverage
- Dental coverage
- Vision coverage
- Retirement and pension plans
- Life assurance
- Disability coverage
- Employee assistance programmes
- Wellbeing resources
- Learning and development opportunities
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
- Administrative
Keywords
- Clinical Trial Associate
- Clinical Research
- FSP
- Regulatory Requirements
- Study Files
- Informed Consent Forms
- Case Report Forms
- Clinical Trial Metrics
- Healthcare
- Documentation
- Compliance
- Clinical Trial Processes
- Sponsor-dedicated
- Mississauga
- Burlington