Trabajos de Medical Regulatory
Reporting
,Regulatory Strategy Project
,Tecnico Regulatory
,Regulatory Strategy Project Lead
,Strategy
TFS HealthScience - Madrid, Community of Madrid, es
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration...
en: es.talent.com - Hace más de 30 días
TFS HealthScience - Madrid, Community of Madrid, es (+1 ubicación)
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration...
en: es.talent.com - Hace más de 30 días
Parexel - Alcobendas, Comunidad de Madrid, es
- Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents...
en: es.talent.com - Hace más de 30 días
PRA - spain, es
You will be provided with a comprehensive and very competitive total reward package that comprises an excellent level of base pay completed with a wide range of variable pay and recognition programs. We...
en: es.talent.com - Hace más de 30 días
TFS HealthScience - Madrid, Community of Madrid, es
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration...
en: es.talent.com - Hace más de 30 días
TFS HealthScience - Barcelona, Catalonia, es (+1 ubicación)
Experienced Medical Writer or Medical Content Reviewer (3-5 years), with a scientific background and degree (PharmD, MD, PhD or Masters), at least 3 years producing or reviewing content for the Pharma/Biotech...
en: es.talent.com - Hace más de 30 días
TFS HealthScience - Barcelona, Catalonia, es (+1 ubicación)
Experienced Medical Writer or Medical Content Reviewer (3-5 years), with a scientific background and degree (PharmD, MD, PhD or Masters), at least 3 years producing or reviewing content for the Pharma/Biotech...
en: es.talent.com - Hace más de 30 días
PSI CRO - Madrid, Community of Madrid, es
Participate in project risk assessment activities, identify program risks, and create and implement mitigation strategies with Clinical Operations Perform medical review of and follow up on incoming SAE...
en: es.talent.com - Hace más de 30 días
PRA - spain, es
Facilitates the review of the documents and ensures that documents are submission-ready and finally approved. When preparing documents you will be directly in contact with QC personnel and publishing specialists...
en: es.talent.com - Hace más de 30 días
PSI CRO - Madrid, Community of Madrid, es
Ensure that the reported data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments PSI Medical Monitors provide medical...
en: es.talent.com - Hace más de 30 días