Lead Clinical Trial Operations Manager Jobs in Germany

The HTA Writer is responsible for providing clinical EUHTA document support to the JCA core team ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process.Provides HTA writing expertise for multiple compounds and/or projec...

Your missionThe Senior Director of Medical Affairs will strengthen and enhance our medical affairs function in supporting pritelivir and our products in development. This senior leadership role will drive medical affairs excellence through strategic oversight of the field-based Medical Science Liais...

About Apheris At Apheris we are building the future of how AI is applied in pharmaceutical R&D.Our federated computing technology enables global pharma companies to collaborate securely on large AI models that accelerate drug discovery without ever sharing their proprietary da...

Multiple locationsRemoteJob DescriptionTake part in a journey committed to innovation and improving lives Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With state-of-the-art biomaterials we produce and market innovative...

YOUR CONTRIBUTIONAs a Regulatory Affairs Manager (m/f/d) you will support regional regulatory strategies approvals and the life cycle management of medicinal products ensuring compliance with regulatory and legal requirements. This position is currently limited to a fixed term of 3 years. Your respo...

Multiple locationsRemoteJob DescriptionTake part in a journey committed to innovation and improving lives Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With state-of-the-art biomaterials we produce and market innovative...

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 Pr...

Why Reesi ExistsEvery year more than 500000 people in Germany are diagnosed with cancer. For many of them a clinical trial could be the best available treatment option yet only 5% ever participate.Not because trials dont exist. But because doctors often dont know which trials are running where and...

Locations: Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and pharmaceutical regulatory consultancy. We specialize in managing registration and approval procedures for chemicals biocides agrochemicals pharmaceuticals and medical devices. With over 160...

Locations: Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and pharmaceutical regulatory consultancy. We specialize in managing registration and approval procedures for chemicals biocides agrochemicals pharmaceuticals and medical devices. With over 160...

Locations: Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and pharmaceutical regulatory consultancy. We specialize in managing registration and approval procedures for chemicals biocides agrochemicals pharmaceuticals and medical devices. With over 160...

Locations: Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and pharmaceutical regulatory consultancy. We specialize in managing registration and approval procedures for chemicals biocides agrochemicals pharmaceuticals and medical devices. With over 160...

Locations: Munich Bad Kreuznach Frankfurt Berlin and Essen. Welcome to Ramboll a global leader in chemical and pharmaceutical regulatory consultancy. We specialize in managing registration and approval procedures for chemicals biocides agrochemicals pharmaceuticals and medical devices. With over 160...

About the OpportunityWe are looking for a Senior Manager Regulatory Project Management to join N26 and play a critical role in strengthening our regulatory resilience. This role is responsible for the trusted coordination execution and oversight of high-impact regulatory projects ensuring consistent...

Zur Geschäftsausweitung suchen wir ab sofort einen engagierten:Regulatory Affairs - Schwerpunkt Medizinprodukte (w/m/d)Vollzeit in KiefersfeldenIhre Herausforderungen als Regulatory Affairs:Sicherstellung der regulatorischen Konformität und Marktfähigkeit von Medizinprodukten gemäß EN ISO 13485 und...