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 cooperative team. At Rho, we cultivate curiosity and embrace new approaches in clinical research. We’re seeking a Clinical Research Associate with a solid 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 on-site monitoring experience
Proficient communication in English and local languages
Robust 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 Ottawa
🏢 RHO
📍 Ottawa