Senior CRA: Lead Across European Trials

Crovelis; Madrid; Presencial; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

CROVELIS is seeking a Senior Clinical Research Associate to independently lead site management, start-up, monitoring and close-out across European trial sites from Madrid. This role emphasizes data quality, patient safety, protocol compliance and timely trial delivery while maintaining a strong quality mindset.

The Senior CRA will collaborate with Clinical Operations, Data Management, Medical and Regulatory teams, ensuring inspection readiness and adherence to ICH-GCP and local regulations.

Formación

• Minimum 5 years of experience in clinical research, including monitoring and site management.
• Experience in pharmaceutical, biotechnology, CRO/service provider or healthcare settings.
• Strong knowledge of ICH-GCP and relevant regulations.

Responsabilidades

• Independently manage assigned clinical trial sites throughout the study lifecycle.
• Conduct site initiation, routine monitoring and close-out visits per monitoring plan and timelines.
• Review source documentation and CRFs for accuracy and protocol compliance.
• Ensure essential study documentation is complete and inspection-ready.
• Identify, assess and manage site issues and operational risks.
• Prepare monitoring visit reports and follow-up letters with clarity and timeliness.
• Provide guidance to junior CRAs and support onboarding and knowledge sharing.

Conocimientos

Clinical monitoring

Site management

Risk-based oversight

Communication

Team collaboration

Project coordination

Educación

Bachelor's or Master's in Life Sciences, Pharmacy, Chemistry, Medicine, Nursing, Biotechnology

Herramientas

Microsoft Office

Clinical trial systems

Descripción del empleo

CROVELIS is seeking a Senior Clinical Research Associate to independently lead site management, start-up, monitoring and close-out across European trial sites from Madrid. This role emphasizes data quality, patient safety, protocol compliance and timely trial delivery while maintaining a strong quality mindset.

The Senior CRA will collaborate with Clinical Operations, Data Management, Medical and Regulatory teams, ensuring inspection readiness and adherence to ICH-GCP and local regulations.