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 innovative 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 innovative community, supporting impactful research in Finland.

📌 Freelance Clinical Research Associate Rho (London)
🏢 RHO
📍 London