Senior CRA — Remote Global Clinical Trials Lead

Worldwide Clinical Trials; Quebec; On-site; CAD 70,000 - 110,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada to manage research activities at study sites and support start-up, data collection and regulatory reporting across multiple therapeutic areas, including Oncology, CNS and Rare Diseases.

You will work with a global team, traveling regionally as needed, while leveraging TMF processes and site management to maintain study timelines and data integrity.

Qualifications

• 5+ years of experience as a Clinical Research Associate or a 4-year university degree or Nursing Degree.
• Experience in Oncology/CNS/Rare Disease is required.
• Candidates must reside in Canada.
• Bi‑Lingual in French and English.

Responsibilities

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including site identification, start-up activities, data reporting and budget/contract support.
• Conduct study initiation visits (SIVs).
• Ensure regulatory compliance and informed consent across sites, with predominantly remote site management.

Skills

Communication

Organization

Independence

Education

4-year university degree

Nursing Degree

Tools

CTMS

EDC Systems

Microsoft Office

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada to manage research activities at study sites and support start-up, data collection and regulatory reporting across multiple therapeutic areas, including Oncology, CNS and Rare Diseases.

You will work with a global team, traveling regionally as needed, while leveraging TMF processes and site management to maintain study timelines and data integrity.