Clinical Research Associate II, Oncology

This is a fully remote position, open to applicants in Canada.

📋 Description

• Perform site selection, initiation, monitoring, and close-out visits.

• Educate site staff on study protocols, EDC systems, and study requirements.

• Ensure the quality of source documentation, maintain data integrity, and facilitate prompt resolution of queries.

• Manage investigator accountability and the gathering of regulatory documents.

• Act as the main point of contact for the site and ensure consistent communication.

• Draft monitoring reports according to standard operating procedures (SOPs) and established timelines.

⛳️ Requirements

• Bilingual in French and English (mandatory).

• A Bachelor’s degree is necessary; ideally in life sciences or a related field.

• Minimum of 1 year of on-site monitoring experience (required).

• Willingness to travel 65–70% of the time.

🏝️ Benefits

• Incentive plans, bonuses, and/or additional forms of compensation.

• Health and wellness benefits.