Clinical Research Associate II (Eastern Canada)

Location: Must live in Ontario or Quebec, Canada; 70–85% travel required and proximity to a major airport is expected.

Company

hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, medical devices, and diagnostics through clinical research services.

What you will do

• Perform on-site and remote monitoring activities for Phase I–IV clinical trials and device trials, including qualification, initiation, interim monitoring, site management, and close-out visits.
• Verify the validity, correctness, and completeness of clinical data in accordance with the protocol, ICH-GCP, ISO 14155, and customer requirements.
• Act as the primary contact for investigative sites and manage query resolution.
• Support Trial Master File activities, Investigators’ Meetings, and other project deliverables within study timelines and budget.
• Identify potential site risks, escalate issues, and coordinate retraining opportunities.
• Plan monitoring visits, complete high-quality trip reports, and actively manage day-to-day deliverables.

Requirements

• Undergraduate degree or international equivalent.
• At least 2 years of clinical research monitoring experience.
• Ability to interact professionally with sites, clients, vendors, and cross-functional teams.
• Accountable, dependable, and strongly committed to high-quality work.
• Ability to complete 8 days on site or monitoring visits per month and travel 70–85%.
• Residence in Ontario or Quebec is required.

Nice to have

• Fluency in French.
• Experience in oncology, pediatrics, or rare-disease clinical trials.

Culture & Benefits

• Flexible work arrangements designed to support work-life balance.
• Opportunities to develop skills and grow professionally.
• Employee ideas and input are encouraged.
• Work focused on advancing medical innovation and improving patient outcomes.