Oncology Clinical Research Associate — Lead Site Trials

Worldwide; Canada; On-site; CAD 70,000 - 90,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada. You will manage site activities across multiple therapeutic areas, including oncology, with remote site management and regional travel supporting regulatory submissions and TMF processes.

The role requires 5+ years as a CRA, a 4-year degree or nursing degree, and the ability to work with minimal supervision while communicating clearly with sponsors and sites.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Experience as a Clinical Research Associate (CRA) with 5+ years in clinical research.
• Experience in Oncology is required.
• Candidates must reside in Canada.
• Willingness to travel regionally.

Responsibilities

• Manage the research activities at sites participating in Worldwide’s clinical research projects.
• Identify potential sites to participate in the research effort and perform start-up activities.
• Support regulatory submissions, TMF management, and budget/contract negotiations.
• Train sites to collect data properly and report safety events; manage site activities during maintenance.

Education

4-year university degree OR Nursing Degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada. You will manage site activities across multiple therapeutic areas, including oncology, with remote site management and regional travel supporting regulatory submissions and TMF processes.

The role requires 5+ years as a CRA, a 4-year degree or nursing degree, and the ability to work with minimal supervision while communicating clearly with sponsors and sites.