Description
We are currently looking for two experienced CRAs, each supporting approximately 0.5 FTE (18 hours/week), with the possibility of combining assignments depending on availability and project needs. The role focuses primarily on monitoring activities across sites throughout Spain.
Responsibilities:
- Perform Interim Monitoring Visits (IMVs) at clinical trial sites
- Ensure protocol adherence and ICH-GCP compliance
- Verify source documents and study data
- Support investigators and site personnel
- Identify and follow up on site issues and action plans
- Collaborate with project teams to ensure successful study delivery
Requirements:
- Minimum 2 years of CRA monitoring experience
- Previous Phase III clinical trial experience
- Strong knowledge of ICH-GCP and clinical trial processes
- Ability to work independently
- Excellent communication and organizational skills
- Fluent Spanish and English
- Willingness to travel within Spain