Clinical Research Associate II: On-Site Monitoring & Study Delivery

Psi CRO; España; On-site; EUR 42,000 - 56,000; Full time

Benefits offered by this job

Permanent contract

Full-time position

Competitive salary

Job summary

PSI CRO in Spain is seeking a Clinical Research Associate II to lead on-site monitoring across Phase II/III studies, ensuring data quality and regulatory compliance. You will build strong relationships with sites and investigators, manage communications with cross-functional teams, and support feasibility studies and regulatory submissions.

The role requires fluent English and Spanish, a Life Sciences degree with a Master’s in Clinical Trials, and at least 1 year of independent on-site

Qualifications

• A Life Sciences degree is required
• A Master’s degree in Clinical Trials is required
• At least 1 year of independent on-site monitoring experience in Spain
• Fluent in English and Spanish

Responsibilities

• Conduct SIV, RMV, COV on-site monitoring visits
• Perform CRF review, source data 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

On-site monitoring

Study coordination

SIV RMV COV visits

CRF review & source data verification

Query resolution

Site management

Vendor coordination

Communication of study progress

Travel readiness

Education

Life Sciences degree

Master’s degree in Clinical Trials

Tools

MS Office

Job description

PSI CRO in Spain is seeking a Clinical Research Associate II to lead on-site monitoring across Phase II/III studies, ensuring data quality and regulatory compliance. You will build strong relationships with sites and investigators, manage communications with cross-functional teams, and support feasibility studies and regulatory submissions.

The role requires fluent English and Spanish, a Life Sciences degree with a Master’s in Clinical Trials, and at least 1 year of independent on-site