Oncology Study Delivery Associate (Hybrid - Mississauga)

ICON Strategic Solutions; Toronto; Hybrid; CAD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Job summary

ICON Strategic Solutions invites applications for a clinical research coordination role in Mississauga, Ontario. The position supports trial administration, regulatory submissions, and cross-functional collaboration to ensure efficient study execution.

Ideal candidates hold a science/healthcare degree and have 2+ years in clinical research, with a strong grasp of regulatory documentation and oncology experience. A hybrid office/home setup is required in Canada.

Qualifications

• Bachelor’s degree in a scientific or healthcare-related field.
• 2 years experience in Clinical Research or an appropriate mix of educational/professional experience.
• Strong understanding of regulatory documentation.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.

Responsibilities

• 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.

Skills

Regulatory documentation

Clinical trial processes

Organizational skills

Communication

Oncology experience

Hybrid work

Team collaboration

Education

Bachelor's degree in a scientific/healthcare field

Job description

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 be doing

• 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

• Bachelor's degree in a scientific or healthcare-related field.
• Two years experience in Clinical Research or an appropriate mix of educational/professional experience
• Must have a strong understanding of regulatory documentation
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Prior experience or strong interest in clinical research.
• Oncology experience required
• Must be comfortable with a hybrid role (office/home) in Mississauga Canada
• Ability to work collaboratively in a fast-paced environment with attention to detail.

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.