Elevate your career at Rho as a Freelance Clinical Research Associate in Finland, where you’ll drive study site performance and data integrity. Engage in diverse challenges with a team-oriented team. At Rho, we cultivate curiosity and embrace new approaches in clinical research. We’re seeking a Clinical Research Associate with a robust background in site monitoring.

Your role will encompass site selection, monitoring, and regulatory compliance to ensure successful study completion within budget. Key Responsibilities:
Manage site monitoring and administration for assigned studies
Conduct comprehensive feasibility assessments and analyses
Perform site initiation and close-out monitoring visits
Facilitate preparation and submissions for Ethics and Regulatory reviews
Collaborate on site contract management and compliance tasks Requirements:
Degree in medicine, pharmacy, nursing, or similar
At least two years of relevant in office monitoring experience
Proficient communication in English and local languages
Strong attention to detail and quality focus
Possession of a driver’s license and willingness to travel Join Rho and take pride in contributing to clinical research excellence in Finland.

📌 Clinical Research Associate Finland Role Toronto
🏢 RHO
📍 Toronto