Description
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.
Key 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
Qualifications
- 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%
The potential base pay range for this role, when annualized, is $84,000.00 - $136,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.