Piedmont Healthcare Inc.

Clinical Trial Associate

Canada, Burlington · Contract

Sponsorship not specified$51k-$63kDetected 2 days ago

AccessibilityClinical TrialsClinical ResearchResearchCommunicationCollaboration

About the role

Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills.
Inclusion and Accessibility ICON is an equal opportunity employer.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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.
We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

Knowledge of clinical trial processes, regulations, and guidelines.
Ability to work collaboratively in a fast-paced environment with attention to detail.
Willingness to travel as required (approximately 10%)

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
Visit our careers site to read more about the benefits ICON offers.
Bachelor's degree in a scientific or healthcare-related field.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.

This listing is sourced directly from Piedmont Healthcare Inc.'s careers page and normalized into a canonical job model.