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 strong 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.
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📌 Clinical Research Associate Finland Role (Ontario)
🏢 RHO
📍 Ontario