Clinical Development Jobs in Germany

Clinical Associate Submissions RegulatoryHomebasedGermanyIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver...

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...

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...

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...

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...

Company OverviewDocusign brings agreements to life. Over 1.5 million customers and more than a billion people in over 180 countries use Docusign solutions to accelerate the process of doing business and simplify peoples lives. With intelligent agreement management Docusign unleashes business-critica...

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...

Advances in scientific and technological research are opening new promising treatments for previously difficult to treat diseases increasing the demand on already constrained healthcare budgets. The challenging economic and political environment is leading Health Technology Assessment (HTA) agencies...

Make your mark for patientsWe are looking foraPatient Affairs Lead Dermatologywho is a results-oriented patient-centric leader that merges strategic advocacy with operational business acumen. You set impulses develop enablement materials steer interfaces and take ownership for outcomes. This is not...

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...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Advise clients project teams sites regulatory agencies and third-party vendors on medical mattersCollaborate with...

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...

People. Passion. Possibilities. Three words that make a world of difference.More than a job. Its a chance to make a real difference.Welcome to AbbVie! As part of an international company with 48000 employees worldwide and around 3000 employees in Germany you will have the opportunity of addressing s...

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...

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...

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...

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...

Job Description SummaryThe Global Head of Clinical Development & Patient Safety Solutions is focused on ensuring that Clinical Development & Patient Safety stakeholders successfully achieve their goals using the technology systems provided. This role involves closely working with Clinical Developmen...

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...