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Clinical Research Associate - Monitoring Experience

Descripción del empleo

Descripción del trabajo

At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes.

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
  • 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 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

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Información extra

Status
Activa
Estudios requeridos
E.S.O
Localización
Madrid
Tipo de contrato
Tiempo completo
Publicado el
16-09-2026
Carnet de conducir
No
Vehículo
No
Carta de motivación
No

Madrid | Tiempo completo | E.S.O

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