Medical Writing Jobs in Spain

We are seeking a dedicated Epidemiology professional to support the design and delivery of high-quality real-world evidence studies in a global cross-functional environment.The role would entail to partner with global clients and cross-functional teams to lead epidemiology for real-world studies acr...

Location: Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction to roleThe Director Clinical Regulatory Writing (Program Lead) provides expert communications leadership across clinical programs and drives effective collaboration and growth within Clinical Regul...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (F...

WHY CHOOSE MEDSIRWe are a Barcelona-based fastest-growing company founded by scientific experts . We are dedicated to the design and management of innovative strategic clinical trials in oncology from study conception to the publication of study results . Together we create the best strategies that...

Please note that fluency in German language is an absolute must for this role.Job Description:We are looking for a highly motivated HTA Analyst / Consultant to be based in Spain and to support health technology assessment (AMNOG) and market access activities in Germany (no travels required). The rol...

THE POSITION: To support a wide range of strategy research analytics and/or value communications projects and the management of project activities other team members and clients.ESSENTIAL DUTIES AND RESPONSIBILITIES:Our employees are tasked with delivering excellent business results through the effo...

POSITION SUMMARYThe Medical Review Excellence Manager will be a key member of the Medical Review (MR) Group by acting as a key partner to in-country Medical Affairs and Marketing colleagues. The MR Manager role does medical and regulatory review aims to minimize compliance risks by ensuring review a...

ARO Platform offers a complete package to Sponsor for managing the necessary activities from start to finish for conducting trials (from phase I to phase IV) and clinical studies.VHIR offers a vacant position within its ARO for a Clinical Project Officer to develop and manage activities in Clinical...

The team & the companyIQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics transformative technology big data resources...

The team & the companyIQVIA is a leading global provider of advanced analytics technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics transformative technology big data resources...

MEDICAL WRITER (with ENGLISHGERMAN mandatory) - REMOTERoleThe Scientific Medical Writer will support the development of scientific content creation:-Medical Information Support: Production of new global standard scientific response content (gSSRC)-Publications Support: Production of abstracts poster...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and Functional Service (FSP) solutions.J...