323 germany English-speaking jobs in Schleswig-Holstein

This role shapes data-driven procurement strategy and execution across a global network. You will build models, dashboards, and external data intelligence to optimize partnerships, unlock savings, and drive resilience. Responsibilities include partnering with procurement teams, delivering analytics for RFPs, and leveraging external datasets to uncover insights.

Leads a global team of cheminformaticians and scientific software engineers in the Synthetic Drug Discovery IT platform. Translates R&D needs into a roadmap and backlog, ensuring successful delivery of initiatives. Manages, mentors, and coaches a team building cutting-edge cheminformatics, modeling, and scientific software solutions.

Provides medical and clinical expertise for new assets, accelerating incorporation through cross-functional collaboration. Leads strategic direction for new molecular entities and line extensions, collaborating with clinical operations, regulatory affairs, market access, and commercial teams.

Senior Statistician II provides statistical expertise for complex design and interpretation of preclinical or clinical programs, regulatory submissions, and commercialization. Analyzes data, develops statistical analysis plans, and coaches less experienced statisticians. Contributes to methodological advances and best practices. Requires a Master's or PhD in Statistics or related field, proficiency in SAS and R, and experience in study design, analysis, and reporting.

Provides medical leadership for preclinical and clinical stage assets in immunology, including SLE, Systemic Sclerosis, Sjogren’s and Rheumatoid arthritis. Leads clinical development activities, including study design, protocol writing, and medical monitoring. Collaborates with internal and external partners to ensure timely execution of studies.

Leads digital health strategy and solution design for pharmaceutical R&D customers, partnering to accelerate clinical development and improve patient outcomes. Manages engagement-level P&L and drives account growth. Requires 8-12+ years of experience in management/healthcare consulting with 5+ years focused on digital health within Pharma R&D.

Leads medical and epidemiologic contributions to research planning and resolves complex issues affecting clinical development. Evaluates and analyzes surveillance, clinical, and real-world data to generate epidemiologic input for product value, risk-benefit, and appropriate use. Leads AstraZeneca personnel, consultants, and contracted specialists in building and management of diverse study types. Prepares proposals for epidemiology, RWE, and outcomes research work packages and manages vendor/CRO selection and oversight. Assists in medical writing, references, and development of dossiers and evidentiary materials for reimbursement/formulary decisions. Advances knowledge of infectious-disease epidemiology and the impact of pharmaceutical product development. Builds a culture of curious leadership, scientific rigor, creativity, and teamwork.

Executive Medical Director for Hematology will lead 2+ clinical development programs from IND to Phase 2/3. Responsibilities include defining clinical strategy, managing benefit-risk profiles, and representing Clinical Development in meetings. Requires MD or equivalent, 7+ years clinical development experience, and experience designing multinational trials.

Associate Principal Packaging Engineer will lead the design, development, and testing of packaging for medical devices and combination products. Responsibilities include developing innovative packaging solutions, generating regulatory documents, and supporting packaging transfer to manufacturing sites. Requires a BSc/PhD in a relevant field and minimum 7 years experience.

The Generative AI Cloud Operations Engineer will design, implement, and manage AI operations systems for clinical trial design, planning, and operational optimization. Responsibilities include integrating LLM proxies, optimizing RAG pipelines, and collaborating with AI Engineers to transition projects into production-grade AI capabilities. The role requires expertise in cloud-native Generative AI deployment methodologies, AWS infrastructure, and regulated industries.

Leads category management, strategic sourcing, and procurement strategies for lab services, including consumables, equipment, people services, and MRO. Develops and executes category roadmaps, collaborates with stakeholders, and manages supplier relationships.

This Front Office role manages daily cash and currency positions across approximately 30 currencies. Responsibilities include liquidity management, money market investments, FX risk management, trade execution, funding coordination, performance reporting, and process improvement. The role requires a degree in a mathematical or finance-related subject, strong Excel skills, and the ability to work accurately under pressure.

Leads a team of formulation scientists in the design and development of oral and inhaled drug products. Responsible for planning and executing formulation development strategies and ensuring regulatory-compliant solutions.

The Global Medical Affairs Leader (GMAL) for Breztri/Trixeo will shape and execute the global medical strategy, driving medical confidence and advocacy. This role supports guideline pull-through and GDMT acceleration, leads the NGP Breztri transition, and orchestrates omnichannel and AI-enabled initiatives. The GMAL provides global oversight of medical affairs, ensuring strategic alignment with therapeutic priorities, lifecycle management, commercial objectives, and scientific standards.

Senior Medical Science Liaison providing scientific expertise in assigned therapeutic areas. Supports pre-launch and launched products, fosters scientific partnerships, and bridges the gap between local and national product strategies.

Medical Science Liaison responsible for executing Medical Affairs Plans for assigned products/indications. Provides scientific support to healthcare professionals and key opinion leaders (HCPs/KEEs) and fosters scientific partnerships within hospitals and institutions.

Secures regulatory licenses for AstraZeneca in Estonia by managing end-to-end regulatory activities for assigned therapeutic areas. Ensures timely submissions, approvals, and lifecycle management in compliance with local and EU requirements. Collaborates with Baltic functions and stakeholders to provide regulatory intelligence, compliance, and strategic guidance.

This strategic role focuses on international regulatory policy for the Asia region (excluding China and Japan). The Director will develop impactful policy and advocacy, collaborating with global, regional, and local experts. Responsibilities include contributing to policy positions, leading stakeholder interactions, and influencing proposed regulations. The Director will also assess the impact of regulatory changes on product strategy and represent AZ in external meetings and conferences.

Leads the global statistical programming function, defining strategy, driving AI innovation, and ensuring quality and compliance. Manages a team of leaders, oversees statistical analysis environments, and collaborates with external partners. Responsible for programming strategy across the drug portfolio, including regulatory submissions.

Develop and lead assigned products throughout their lifecycle. Understand market needs, analyze data, and formulate brand strategies. Drive key initiatives, monitor performance, and lead sales team objectives.