Descripción de la oferta
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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