Freelance Clinical Research Associate (CRA) – Spain

About the role

IQVIA Biotech is looking for two experienced freelance CRAs to support two Phase III clinical studies in Spain. Each position is about 0.5 FTE (roughly 18 hours per week), with the possibility of combining assignments depending on availability and project needs. The role focuses mainly on monitoring activities across sites throughout Spain, with nationwide travel.

Key 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

Required profile

• 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
• Fluent Spanish and English
• Willingness to travel within Spain

The start date is ASAP and the duration is approximately 6 months, with around 2-3 site visits per month across roughly 10 sites. Applications are made through the IQVIA careers site.