Senior Clinical Research Associate/CRA - FSP Canada Operations – Project Management

Key Responsibilities:

• Conduct site monitoring activities including initiation, routine visits, and close-out per Study Monitoring Plan and regulations.
• Act as primary liaison for investigator sites, ensuring effective communication and resolving issues to maintain trial timelines.
• Support site activation, recruitment, and enrollment in collaboration with study teams and site care partners.

Qualifications:

• Minimum 3+ years of clinical research monitoring experience, preferably in oncology or complex therapeutic areas.
• Strong knowledge of ICH-GCP, clinical trial operations, and FDA/local regulations.
• Bachelor’s degree in life sciences or related field; nursing, pharmacy, or medical background preferred.

Work Environment:

• This is a field-based remote role requiring up to 60-80% travel across Canada.
• You will work with global clinical trials and cross-functional teams, driving site performance and data quality.
• You must be able to manage multiple sites independently and have a valid driver’s license and passport for travel.