Clinical Research Associate I: Global Trials & Travel

KCR Placement; Barcelona; On-site; EUR 42,000 - 60,000; Full time

Benefits offered by this job

Annual leave

Health insurance options

Retirement planning

Employee assistance program LifeWorks

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate I to join our sponsor-dedicated team. You will contribute to clinical trial monitoring across programmes, delivering high-quality monitoring work and maintaining robust study documentation.

Responsibilities include coordinating study setup and monitoring, handling sponsor queries, and collaborating with investigators and site staff to ensure patient safety and regulatory compliance. Travel of about 60% is required.

Qualifications

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the ability to review medical data.
• Excellent written and verbal communication in English.
• Willingness to travel approximately 60%.

Responsibilities

• Deliver clinical trial monitoring work to a high standard across studies.
• Coordinate setup, monitoring, and study documentation; complete accurate status reports.
• Participate in sponsor-generated queries and support study cost efficiency; assist in feasibility/proposal reviews.

Skills

English proficiency

Communication skills

Team collaboration

Travel willingness

Education

University degree in medicine or science

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate I to join our sponsor-dedicated team. You will contribute to clinical trial monitoring across programmes, delivering high-quality monitoring work and maintaining robust study documentation.

Responsibilities include coordinating study setup and monitoring, handling sponsor queries, and collaborating with investigators and site staff to ensure patient safety and regulatory compliance. Travel of about 60% is required.