264 English-speaking jobs in Schleswig-Holstein

Development Scientist III will oversee outsourced analytical testing, ensuring timely, compliant, and high-quality delivery. Responsibilities include managing laboratory investigations, reviewing protocols, and supporting analytical method lifecycle. Requires a Master's or Ph.D. in a relevant field with 6-10 years (Ph.D.) or 15+ (M.S.) years of experience.

Develop and lead assigned products to their optimal potential throughout the product lifecycle. Responsibilities include market research, formulating and implementing marketing strategies, and collaborating with sales teams. Requires a science or marketing background and at least 3 years of experience in Brand Management within Specialty Care. Fluency in English and strong communication skills are essential.

The Field Medical Writer will develop, write, and update a standardized hyperkalemia treatment protocol across 8-10 hospitals. The role involves collaborating with key external experts and hospital stakeholders to harmonize practices, incorporate evidence-based recommendations, and drive protocol adoption.

The Director, Process Safety & SIF Prevention designs, governs, and delivers the global strategy to eliminate serious injuries and fatalities across Operations, R&D, and Commercial environments. This role leads a global transformation agenda that sets new standards for risk reduction, competency, technology integration, and safety-critical decision making.

Shape intuitive SAP experiences by building Fiori applications and scalable CAP services. Design, develop, and support on-premise and cloud SAP Fiori, UI5, and CAP applications across multiple functional areas. Architect and develop custom Fiori applications using UI5 and CAP, integrating with custom ABAP where needed. Design and deploy AI-powered solutions on SAP BTP, integrating Generative AI into applications, automation, and integrations. Implement extensions in the ABAP environment and use low-code/no-code tools to adapt SAP LoB solutions. Produce technical design documents, establish coding standards, and implement automated testing. Facilitate functional discussions with key users, translate requirements into scalable designs, and manage application security and optimization. Stay updated with the latest SAP UI5/Fiori trends and standard methodologies.

Leads national sales objectives for assigned oncology brand, ensuring alignment with AstraZeneca's strategic goals. Develops and executes brand and tactical plans, leveraging analytical skills for customer segmentation and data-driven decision making. Builds high-performing teams and fosters a culture of growth and innovation.

Leads the design, development, and deployment of analytics solutions and data products. Collaborates with global and regional data leads to define and execute the data and analytics roadmap. Owns and leads end-to-end project delivery and acts as MEA Data Architect.

Leads safety scientist activities across multiple product portfolios, manages regulatory filings, and represents global patient safety at inspections.

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.

Leads global medical strategy for Oncology brands, ensuring alignment between tumor-level and brand-level strategies. Develops and executes medical plans, including evidence generation, scientific communications, and patient-centric initiatives. Collaborates cross-functionally and externally, representing AstraZeneca at scientific events. Provides medical leadership for HA/IRB interactions and GMA-sponsored studies.

Senior District Business Manager will develop and execute district operational plans, drive brand plan execution, and analyze district performance. The role requires a minimum of 2 years in the position, sales performance above 90% or national performance, and a DBM Proficiency Level rating of at least 3.5.

Leads the development and delivery of health economic models for global HTA submissions. Contributes to the development of HMS tools, guidance documents, and publications. Manages modeling projects and builds partnerships with cross-functional teams. Requires a bachelor's or postgraduate degree in a quantitative field and 5+ years of experience applying modeling expertise to HTA submissions.

The Global Medical Director Cardiology provides strategic planning and leadership for Amyloidosis indications and the expanding pipeline portfolio. This role requires matrix leadership and collaboration with global functions, including Commercial, Clinical Development, and Regulatory Affairs. Responsibilities include representing GMA at Global Program Teams, developing global medical plans, mentoring scientific communication teams, and leading phase 3b/4 clinical studies.

The Associate Director – Cell Therapy Territory Operations Manager provides operational and clinical guidance for cell therapy trials and commercial products. The role leads site activation, ongoing operational oversight, and builds patient-centered service lines. The position requires 8+ years of cell therapy experience with progressive leadership and expertise in service lines, quality metrics, and cell therapy standards/regulations.

Executes diagnostics strategy within assigned therapeutic areas, translating objectives into actionable plans. Drives project implementation, builds partnerships with stakeholders, and monitors progress. Communicates scientific concepts, generates evidence, and collaborates with cross-functional teams.

The Associate Director, Country Operations Management reports to the Director, Study Start-Up and Site Partnership. This role is responsible for the successful delivery of all assigned operational trial activities, ensuring timelines, operational procedures, quality standards, SOPs, and guidelines are consistently met. The AD COM leads and develops a dedicated functional group within the local Country Operations Management team, oversees planning and resource utilization, and sets objectives for their team. They also contribute to regional and global initiatives as delegated.

The Senior Regulatory Affairs Director (SRAD) leads a Global Regulatory Strategy Team (GRST) developing and implementing global strategies for complex oncology programs. The SRAD represents Regulatory Affairs on Global Product Teams (GPTs) and owns the delivery of all regulatory milestones.

Leads early Phase I-II global clinical trials for kidney disease compounds, ensuring scientific integrity, patient safety, and regulatory compliance. Provides clinical leadership to cross-functional teams, integrating preclinical insights into clinical plans. Contributes to regulatory interactions and documentation.

Leads statistical design and strategy across product development, ensuring transparency, quality, and timely delivery. Provides leadership and direction to internal and external statisticians, mentoring and supporting their technical development. Collaborates with CROs, health authorities, and advisory boards. Maintains deep knowledge of statistical methodology and promotes innovative approaches. Influences statistical strategy and decision-making at internal governance bodies.

Develop and implement Brand Strategic Plans, including market share and sales targets. Gather and interpret market analyses, SWOT, competitor analyses, and sector developments. Lead strategic decisions to enhance business performance.