Senior Clinical Research Associate — Remote Spain

ICON Clinical Research

España

A distancia

EUR 52.000 - 68.000

Jornada completa

Hace 3 días
Sé de los primeros/as/es en solicitar esta vacante
Generador de candidaturas

Destaca en este puesto — crea un currículum adaptado y una carta de presentación en aproximadamente un minuto.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Various annual leave entitlements
Health insurance offerings
Retirement planning offerings
Employee assistance programme
Life assurance
Flexible benefits

Descripción de la vacante

ICON Plc is seeking a Senior Clinical Research Associate to work on a home-based basis in Spain. You will oversee clinical trial monitoring activities, ensuring compliance with protocols, regulatory requirements, and GCP standards while supporting site staff and cross-functional teams.

The role emphasizes independent work, training of staff, and maintaining strong relationships with sites to drive quality and timely data collection.

Formación

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Extensive experience as a Clinical Research Associate, with understanding of trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects with strong organizational skills.
  • Experience with monitoring practices and data integrity in clinical trials.
  • Excellent communication and stakeholder management in a complex environment.
  • Willingness to travel approximately 60%.

Responsabilidades

  • Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
  • Conduct site visits to assess performance, resolve issues, and support successful trial execution.
  • Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Provide training and guidance to site staff and other CRAs to maintain high standards of trial conduct.
  • Build and maintain effective relationships with site personnel and stakeholders for smooth operations.

Conocimientos

Clinical trial monitoring
Data integrity
Site management
Communication skills
Problem-solving
Travel readiness

Educación

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Herramientas

Clinical trial software

Descripción del empleo

ICON Plc is seeking a Senior Clinical Research Associate to work on a home-based basis in Spain. You will oversee clinical trial monitoring activities, ensuring compliance with protocols, regulatory requirements, and GCP standards while supporting site staff and cross-functional teams.

The role emphasizes independent work, training of staff, and maintaining strong relationships with sites to drive quality and timely data collection.

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