Senior Clinical Research Associate position based in Spain overseeing clinical trial monitoring and site management. The role involves ensuring protocol adherence, regulatory compliance, and quality standards while leading monitoring activities and supporting cross-functional teams in a sponsor-dedicated model.
Responsibilities
Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
Conduct site visits to assess performance, resolve issues, and provide operational support
Collaborate with cross-functional teams on data collection, quality, and reporting
Train site staff and other CRAs to maintain clinical trial conduct standards
Build relationships with site personnel and stakeholders to facilitate trial operations
Requirements
Bachelor's degree in scientific or healthcare-related discipline
Extensive Clinical Research Associate experience with clinical trial process knowledge
Ability to manage multiple sites and projects with strong organizational skills
Expertise in monitoring practices, data integrity, and clinical trial software
Excellent communication and stakeholder management capabilities
Willingness to travel approximately 60% as required

📌 Senior CRA (España)
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📍 España