CRA II: On-Site Monitoring & Coordination

SmartRecruiters, Inc.; Madrid; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Competitive salary

Team collaboration

Friendly colleagues

Onboarding courses

Well-established office

Job summary

PSI is a leading Contract Research Organisation delivering quality and on-time services across therapeutic indications. The Clinical Research Associate II will manage site relationships, ensure data integrity, and support regulatory submissions.

Role focuses on patient safety, data quality, and collaboration with internal teams and vendors in a dynamic Spain-based environment. Travel and bilingual English/Spanish communication are required.

Qualifications

• Degree in Life Sciences and a Master's in Clinical Trials are required.
• At least 1 year of independent on-site monitoring experience in Spain.
• Experience in Phase II and/or III monitoring visits.
• Full working proficiency in English and Spanish.
• Proficiency in MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel.

Responsibilities

• Conduct and report SIV, RMV, COV on-site monitoring visits.
• Perform CRF review, source document verification and query resolution.
• Be responsible for site communication and management.
• Be a point of contact for in-house support services and vendors.
• Communicate with internal project teams regarding study progress.
• Participate in feasibility research.
• Support regulatory team in preparing documents for study submissions.
• Prepare and participate in audits and inspections.

Skills

MS Office

Communication

Teamwork

Travel

Education

Bachelor's in Life Sciences

Master's in Clinical Trials

Job description

PSI is a leading Contract Research Organisation delivering quality and on-time services across therapeutic indications. The Clinical Research Associate II will manage site relationships, ensure data integrity, and support regulatory submissions.

Role focuses on patient safety, data quality, and collaboration with internal teams and vendors in a dynamic Spain-based environment. Travel and bilingual English/Spanish communication are required.