Empleos de Discover International en España

A specialized radiopharmaceutical company is seeking a Chief Medical Officer (CMO) to lead global medical strategies and provide clinical leadership. · Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su s ...

El auditor de calidad GCt es responsable de garantizar que los sistemas eClinical cumplan con las normas regulatorias. · Servicios clave: · Liderar actividades de validación para sistemas eClinical. · Especificaciones del puesto: · - 4 días a la semana presenciales en Madrid. · - ...

Chief Medical Officer (CMO) – Radiopharmaceuticals · No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. · Location : Remote (Europe or United States) · About the Company · A rapidly growing diagnostic ...

Job Summary: · The Chief Medical Officer (CMO) will provide global medical, clinical, and scientific leadership across the diagnostic radiopharma portfolio. · ...

Job Description · This role supports pharma, biotech, and medical device clients across Europe and USA with challenging regulatory issues. · Provide advice to clients on quality aspects of drug development and regulatory requirements. · Ensure that the content of CMC work-package ...

A leading regulatory consulting firm in Spain is looking for a Senior CMC Regulatory Consultant to provide expert advice on quality aspects of drug development. This remote role requires significant experience in regulatory filings and CMC documentation. · Key Responsibilities: · ...

Join our team at discover-international · About Us · We are looking for an experienced Computer System Validation Engineer for a 6-month freelance project · Familiarity with regulatory expectations. · ...

**Job Summary:** · A specialized radiopharmaceutical company is seeking a Chief Medical Officer (CMO) with extensive experience in diagnostic radiopharmaceuticals and senior leadership in biotech or pharma, with proven clinical development, regulatory engagement, and medical str ...

Clinical Project Leader · Lead and oversee Phase I PK/PD, PD, and BE clinical trials. · Coordinate cross-functional teams to ensure regulatory compliance. · ...

Clinical Project Manager · About Us: · We are working with a forward-thinking pharmaceutical company specializing in early-phase clinical development and bioequivalence studies for generic pharmaceuticals. · Lead planning execution close-out phase I PK/PD BE clinical studies · Ma ...

A key role in ensuring compliance with GxP regulations involves supporting validation activities for computer systems used in pharma or biotech environments. Ideal candidates will have experience with CSV documentation and execution of IQ/OQ/PQ checks. · Key Responsibilities: · ...