Empleos de Ema

This Director role at AstraZeneca involves shaping global regulatory strategy for cell therapy programs across oncology, immune-mediated, and rare diseases.

IQVIA's Regulatory Science and Strategy group is hiring a Principal (Director-level) in Madrid to lead regulatory strategy engagements and support real-world evidence studies for regulatory…

This is a senior medical writing role within IQVIA's FSP (Functional Service Provider) model, embedded in a sponsor's workflows.

The QA Validations Expert will lead validation activities for manufacturing, laboratory, and computerized systems in Madrid, ensuring GMP and regulatory compliance.

The Quality Assurance Specialist will ensure compliance with FDA, EMA, and GMP standards across pharmaceutical manufacturing and laboratory operations.

The Associate Director Senior Study Lead leads the cross-functional clinical trial team, managing assigned clinical studies end-to-end from planning through execution and reporting.

CTI Clinical is hiring a Clinical Director for its Bilbao laboratory, responsible for scientific and administrative oversight of specialty testing, quality management, and personnel.