About The Position

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. IQVIA Biotech 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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