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 on-site monitoring experience
• Solid 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.
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