Clinical Trials Associate – US/Canada (Impactful Work)

Worldwide Clinical Trials; Canada; On-site; CAD 32,000 - 65,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Trials Associate in Canada to provide administrative and project tracking support to the clinical project team. You will ensure timely and accurate tasks across assigned projects and support the Project Delivery services.

Ideal candidates bring strong English communication, multi-tasking ability, attention to detail, and proficiency with MS Office applications. This role involves handling project documentation and site files with precision.

Qualifications

• Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
• Skill sets and proven performance equivalent to the above

Responsibilities

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
• Maintain and quality audit to assure the most recent revisions of documents are on project portals
• Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
• Maintain version and quality control of project documentation and submit to trial master file
• Assist with the tracking and maintenance of project related information, including site medical question and answer log

Skills

MS Office

Attention to detail

Project coordination

Education

Degree or equivalent

Tools

Outlook

Word

Excel

PowerPoint

Job description

Worldwide Clinical Trials is seeking a Clinical Trials Associate in Canada to provide administrative and project tracking support to the clinical project team. You will ensure timely and accurate tasks across assigned projects and support the Project Delivery services.

Ideal candidates bring strong English communication, multi-tasking ability, attention to detail, and proficiency with MS Office applications. This role involves handling project documentation and site files with precision.