Clinical Research Associate II: Global Trials & Site Monitoring

IQVIA Inc; Madrid; On-site; EUR 30,000 - 42,000; Full time

Job summary

IQVIA Spain is seeking a junior Clinical Research Associate to join our Sponsor dedicated team in Madrid or Barcelona. You will gain experience across therapeutic areas while building a solid career within an international company.

Your responsibilities include site visits (initiation, monitoring, close-out), assisting with recruitment planning, and ensuring regulatory compliance with GCP/ICH guidelines. Fluency in Spanish and English is required.

Qualifications

• University degree in a scientific field or health care.
• Excellent command of Spanish and English.
• Very good computer skills including MS Office.
• Strong organizational, time management and problem-solving abilities.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate site practices for regulatory compliance (GCP/ICH).
• Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions.
• Collaborate with study sites and client representatives.

Skills

Spanish

English

Communication

Teamwork

Education

University degree in scientific discipline or health care

Tools

MS Office

Driver's license class B

Job description

IQVIA Spain is seeking a junior Clinical Research Associate to join our Sponsor dedicated team in Madrid or Barcelona. You will gain experience across therapeutic areas while building a solid career within an international company.

Your responsibilities include site visits (initiation, monitoring, close-out), assisting with recruitment planning, and ensuring regulatory compliance with GCP/ICH guidelines. Fluency in Spanish and English is required.