Clinical Research Associate — Global Trials & Training

Medpace; Madrid; Presencial; EUR 42.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive pay

Health benefits

Retirement benefits

Paid time off

Mentorship and training

Flexible work arrangements after培训

Descripción de la vacante

Medpace in Madrid is seeking a Clinical Research Associate to support site management and data integrity across therapeutic areas. You will engage in site qualification, monitoring, and regulatory activities to ensure compliant, high-quality trials.

A collaborative, global environment offers training and growth opportunities. Expect approximately 60-80% travel, on-site work, and frequent cross-functional collaboration.

Formación

• Minimum university degree in a health or life science related field.
• Excellent verbal and written English and Spanish.
• Outstanding communication and presentation skills.
• Detail-oriented with strong time management.

Responsabilidades

• Conduct qualification, initiation, monitoring, and closeout visits in line with the protocol.
• Communicate with site staff including coordinators and physicians.
• Verify investigator qualifications, training, facilities, and resources.
• Verify medical records and source data against case report forms and ensure adherence to GCP and SOPs.
• Ensure enrolling only eligible subjects and perform regulatory document reviews.
• Manage device/investigational product/drug accountability and inventory.
• Review adverse events and related data for accuracy and compliance.
• Assess site recruitment/retention and suggest improvements.
• Prepare monitoring reports and follow-up letters with notable findings and recommended actions.

Conocimientos

Communication

Time management

Microsoft Office

English

Spanish

Travel readiness

Educación

Bachelor's degree in health or life sciences

Herramientas

Microsoft Office

Descripción del empleo

Medpace in Madrid is seeking a Clinical Research Associate to support site management and data integrity across therapeutic areas. You will engage in site qualification, monitoring, and regulatory activities to ensure compliant, high-quality trials.

A collaborative, global environment offers training and growth opportunities. Expect approximately 60-80% travel, on-site work, and frequent cross-functional collaboration.