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 on-site 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. #J-18808-Ljbffr