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 collaborative 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 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. #J-18808-Ljbffr

📌 Clinical Research Associate Finland Role (Winnipeg)
🏢 RHO
📍 Winnipeg