Clinical Trials Associate (US/Canada) — Global Impact

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

Job summary

Worldwide Clinical Trials (Canada, Alberta) is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed timely and accurately. You will arrange and track system access, audit documents on project portals, and assist with preparation and shipment of trial documentation, including the Investigator Site File.

A degree plus at least one year of related experience is required, with strong English skills and

Qualifications

• Degree or equivalent experience in a related field.
• Minimum of 1 year in a related role.
• Experience in clinical research administration is a plus.

Responsibilities

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
• Maintain and quality audit to assure latest revisions of documents 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 tracking and maintenance of project information, including site medical Q&A log

Skills

MS Office

Time management

Attention to detail

Communication skills

Education

Bachelor's degree or equivalent

Job description

Worldwide Clinical Trials (Canada, Alberta) is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed timely and accurately. You will arrange and track system access, audit documents on project portals, and assist with preparation and shipment of trial documentation, including the Investigator Site File.

A degree plus at least one year of related experience is required, with strong English skills and