Clinical Trials Jobs in Germany

Our client global Leader in the Pharmaceutical Industry is looking for an experienced Medical Science Liaison specialized in Oncology.The role will be based remotely (ideally from Munich) with frequent travelling at a regional level.Your activities will consist in establishing scientific collaborati...

Your missionThe Medical Science Liaison (MSL) is a field-based scientific and clinical expert required to reside within the assigned geographic territory (Northeast Southeast Midwest South Central Mountain/Southwest or West Coast) and serves as the primary communicator of our science for that region...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAssistant CRA - Germany2 Year Fixed Term contractAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our c...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH) a serious liver disease that can progress to cirrhosis liver failure need for liver transplantation and premature mortality. Every member of our Madrigal team...

Why IQVIAThis role will be dedicated to one of IQVIAs largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These spon...

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...

This is what you will do:The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexions scientific platform and product/s across the product/s life cycle. He/she is a peer scientific expert who communicates accurate...

This is what you will do:The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time cost and quality objectives accordin...

We are seeking a talented and motivated Scientific intern/working student regulatory affairs (m/f/d) to contribute to apply test characterize Open Systems Pharmacology PBPK platform in light of regulatory requirements.ESQlabs is an innovative internationally acting Contract Research Organization and...

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confidentiality agreem...

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory s...

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...

Clariness is looking for a Team Lead Project and Operations Management (f/m/d) based in Berlin or Hamburg.- Full-time; unlimited -About the role:In this role you will be responsible for leading project teams and ensuring the successful delivery of clinical trial recruitment projects across multiple...

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 ApherisAt 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 data. By powering multi-pa...

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...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

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...