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Clinical Research Associate - Monitoring Experience Required

Descripción del empleo

At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome)

  • Minimum of 4 years of advanced experience in clinical research monitoring
  • Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud.
  • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., Excellent communication skills for site interaction, training, and issue resolution
  • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members
  • Hands-on experience with monitoring systems, source data verification, and compliance tracking
  • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring)
  • Fluent communication in English and Spanish (Catalan is preferred, French optional)
  • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out
  • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements
  • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity
  • Conduct site training, initiation visits, and support audit and inspection readiness
  • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams
  • Support xkdbapo investigator meetings, coordinator meetings, and deliver presentations or training sessions when required
  • Mentor junior CRAs and contribute to process improvements and best practices
  • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts

Hybrid working model with flexibility

Opportunities for growth and professional development

Clinical Research Associate - monitoring experience required Arbo, galicia, Spain

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Información extra

Status
Activa
Estudios requeridos
E.S.O
Localización
Arbo
Tipo de contrato
Tiempo completo
Publicado el
21-09-2026
Carnet de conducir
No
Vehículo
No
Carta de motivación
No

Tiempo completo | E.S.O

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