About The Position

IQVIA is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is home-based in Eastern Canada and requires fluency in both French and English. The CRA II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out.

Requirements

  • Bilingual in French and English (Required)
  • Bachelor’s Degree required. Preference in life sciences or related discipline.
  • Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • At least 1 year of onsite monitoring experience (Required)
  • Ability to travel 65–70%

Responsibilities

  • Conduct site selection, initiation, monitoring, and close-out visits
  • Train site personnel on study protocols, EDC systems, and study requirements
  • Ensure high-quality source documentation, data integrity, and timely query resolution
  • Oversee IP accountability and regulatory document collection
  • Serve as the primary site contact and maintain regular communication
  • Prepare monitoring reports following Standard Operating Procedures and timelines
  • Support investigator meetings and collaborate with CTMs/Lead CRAs

Benefits

  • health and wellness benefits
  • other benefits
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