Senior Clinical Research Associate

📋 Description

• Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the
• Assist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by
• May act as Feasibility Associate.
• Train site staff in all study procedures.
• Conduct periodic monitoring visits, including completion of monitoring visit report. Review at each
• Conduct source data verification and in-house review of clinical data and ensure timely resolution

🎯 Requirements

• University Degree in scientific, medical or paramedical disciplines.
• At least eight (8) years of clinical research experience, including proven experience as a Clinical
• Previous experience working for a CRO is required.
• Experience with a broad range of therapeutic areas is desired.
• Strong knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory
• Fluent in English and Spanish - required.

🎁 Benefits

• Full-time, permanent position
• Remote position based in Spain
• Opportunity to work across a diverse portfolio of projects
• Professional development and excellent work-life balance
• Quality-focused, collaborative 'one-team' culture
• Meaningful impact on global healthcare