Senior Clinical Research Associate - Spain
Core
Independent clinical trial monitoring across oncology, neurology, and infectious diseases to ensure site compliance, data quality, and patient safety.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data integrity and regulatory compliance for innovative therapies
Domain
Clinical Research / Life Sciences
Required skills
Clinical trial monitoring, GCP/ICH guidelines, CRF review, CAPA planning, site contract negotiation, risk identification, scientific journal analysis, data management systems
Preferred skills
Oncology, neurology, or infectious diseases experience
Technologies
Data management systems
Responsibilities
Perform routine site visits (pre-study, initiation, interim, closeout), manage assigned sites for compliance and enrollment, independently review CRFs and resolve queries, prepare CAPA plans, negotiate study budgets with investigators, prepare documents for EC submissions
Seniority
Mid-Senior, hands-on IC