Clinical Research Associate — Impactful Trials & Data Quality

PulseMedica; Mississauga; Hybrid; CAD 60,000 - 75,000; Full time

Benefits offered by this job

Group RRSP

Medical benefits

Job summary

PulseMedica is seeking a Clinical Research Associate to drive trial execution across sites in Canada and the US. You will manage site activation, monitoring visits, and TMF while ensuring data quality and regulatory compliance.

The role emphasizes collaboration with study teams to implement processes and improve trial conduct. The ideal candidate has 1–3 years of CRA experience, strong written communication, and a proactive, detail-oriented mindset.

Qualifications

• Experience in managing clinical trial activities from startup to closeout.
• Knowledge of GCP guidelines and ethics board policies.
• Strong written communication and ability to present complex information clearly.
• Proven ability to build relationships with site personnel and stakeholders.

Responsibilities

• Execute core clinical operations activities with site management, SIV, IMV, TMF maintenance.
• Review site contracts, budgets, and ethics submissions as part of trial setup.
• Maintain relationships with study personnel and drive issue resolution.
• Ensure data accuracy through SDR/SDV and monitoring activities (on-site/remote).
• Analyze data for inconsistencies and risks; develop mitigation plans.
• Support training for colleagues as requested and ensure compliance with regulations.

Skills

Clinical operations

Site management

Documentation

Regulatory familiarity

Communication

Travel 60%

Education

Bachelor’s degree in biomedical sciences

MSc thesis-based preferred

Job description

PulseMedica is seeking a Clinical Research Associate to drive trial execution across sites in Canada and the US. You will manage site activation, monitoring visits, and TMF while ensuring data quality and regulatory compliance.

The role emphasizes collaboration with study teams to implement processes and improve trial conduct. The ideal candidate has 1–3 years of CRA experience, strong written communication, and a proactive, detail-oriented mindset.