Clinical Research Associate Oncology Trials

Position: Clinical Research Associate for Oncology Trials
Advance your career with Prevail as a Clinical Research Associate specializing in oncology trials in Canada. This role integrates your skills in site monitoring and trial management for Breast Cancer studies.

As a Clinical Research Associate, you will perform monitoring activities for Phase I-IV trials while working remotely or on-site across British Columbia, Ontario, and Quebec. Your responsibilities will include managing site compliance with ICH-GCP guidelines and industry standards. You can apply your judgment to elevate site performance and tackle issues effectively.

Key Responsibilities:

• Conduct interim monitoring and site close-out visits

• Verify informed consent has been obtained

• Document all activities in compliance with SOPs

• Ensure safety and integrity of clinical data

• Facilitate investigator meetings and training sessions

Requirements:

• Strong knowledge of GCP and regulatory requirements

• Excellent skills in Word, Excel, and presentations

• Proven customer service orientation

• Ability to travel regularly, up to 65%

• Bachelor’s degree in a relevant field preferred

Utilize your monitoring expertise with Prevail to drive successful clinical trials focused on oncology.
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