Explore a unique freelance opportunity at Rho as a Clinical Research Associate in Finland. You’ll manage site operations, ensure data quality, and contribute to creative research projects. Rho is redefining the CRO landscape with a culture built on collaboration and curiosity.

We are looking for a Clinical Research Associate with at least two years of site monitoring experience. In this role, you will handle site administration, feasibility studies, and compliance with ICH-GCP Guidelines, working closely with our supportive and energetic team. Key Responsibilities:
Oversee site administration and monitoring for clinical studies
Conduct feasibility assessments for sites and countries
Execute site initiation and close‑out visits




Prepare submissions to Ethics Committees and Regulatory Authorities
Assist in site contract management and compliance Requirements:
University degree in medicine, pharmacy, nursing, or related field
Minimum two years of in office monitoring experience
Strong communication skills in English and local languages
Attention to detail and commitment to high-quality standards
Valid driver’s license and travel capability Become a vital part of Rho's creative community, supporting impactful research in Finland.

📌 Freelance Clinical Research Associate Rho Ottawa (Canada)
🏢 RHO
📍 Canada