265 English-speaking jobs in Schleswig-Holstein

Leads and implements strategies to drive sales and secure contracts with pharmaceutical companies. Identifies and capitalizes on new business opportunities, developing consultative initiatives that position Evinova as a trusted partner in digital clinical solutions.

Develops brand forecasts (revenue, volume, and patients) for strategic brands and/or early assets. Works closely with the GIBEx/GA&I Forecast Leader and Commercial teams. Maintains up-to-date forecast models and leads forecasting, business planning processes. Identifies key business issues impacting forecasts and incorporates primary research results. Develops new product introduction volume forecasts and supports continuous improvement of forecasting capabilities.

As Principal Engineer Continuous Direct Compression (CDC), you will lead the design, development, and optimization of CDC processes for late-stage oral solid dose drug product development projects. You will build predictive tools, digital twins, and CDC process development capability, collaborating with diverse scientific teams.

Leads the Diagnostics Center of Excellence strategy, driving innovation from discovery through lifecycle management. Develops end-to-end diagnostic approaches for precision medicine. Manages clinical trial diagnostic strategies, regulatory submissions, and external partnerships.

Provides medical and scientific input to preclinical and clinical stage assets focused on Rheumatology/Clinical Immunology. Responsible for clinical development in cross-functional teams to support early phase clinical development activities, including clinical study design, protocol writing, and medical monitoring. Requires experience in Rheumatology drug development, including trials in diseases such as systemic lupus erythematosus and Rheumatoid Arthritis.

Leads the end-to-end external scientific engagement strategy for AstraZeneca's Cardiovascular, Renal & Metabolism (CVRM) therapeutic area. Develops and executes strategies for Key Opinion Leader (KEE) engagement, professional societies, advocacy groups, and external medical education providers. Serves as the external scientific persona for CVRM, building a unified interface to elevate AstraZeneca's scientific leadership. Builds and leads a global ESE team, ensuring consistent execution across regions. Collaborates cross-functionally with Medical Affairs, R&D, and Commercial teams to align priorities and improve value. Owns the CVRM BPM ESE budget and partners with agencies to elevate AstraZeneca's scientific standing.

Leads and manages a medical team, developing and executing medical evidence plans to support oncology products. Oversees medical affairs direct reports, including field and headquarters teams. Accountable for medical insight generation and opinion leader engagement. Requires a sophisticated scientific degree and 7+ years of relevant clinical experience.

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.

Clinical Procurement Partner will act as a dedicated business partner to Clinical Operations within R&D Global Procurement. This role requires clinical trial fluency and procurement understanding to support cross-functional alignment and enable proactive procurement planning. The position will translate Therapy Area strategy and clinical plans into procurement insights and demand forecasts.

Staff Engineer will build Agentic AI solutions for oncology research, developing and supporting tools for genomics, pathology, and clinical trials. Requires a relevant graduate degree and 10+ years of experience in software engineering, data science, or bioinformatics. Must have hands-on experience with Agentic AI systems and strong Python and/or TypeScript skills.

The Director Quality Assurance APAC will manage the strategic development and delivery of a GXP risk-based quality assurance program. Responsibilities include leading and conducting complex audits, providing quality and compliance advice to stakeholders, and overseeing regulatory GxP inspections.

Leads formulation and process development of injectable drug products for Alexion's diverse portfolio, spanning synthetic, peptide, genomic medicine, and protein-based modalities. Manages budget, partners, and ensures development of portfolio projects in a phase-appropriate manner. Collaborates with internal and external partners on technology transfer and drug product engineering. Provides subject matter expertise for regulatory filings and interactions.

Communications Executive will manage digital and social media platforms, execute events, and support internal communications initiatives. The role requires 4+ years of corporate communications experience, strong communication skills, and proficiency in MS Office applications.

Group Medical Manager to lead medical strategy and evidence generation for breast cancer therapies. Requires a medical degree, minimum 5 years of medical affairs experience, including 2 years in oncology and 2 years in a managerial role. Excellent communication, leadership, and facilitation skills are essential.

Marketing Excellence Specialist/Manager will develop and execute launch and marketing capability development plans. The role involves analyzing insights, building strategic plans, and monitoring impact. Responsibilities include collaborating with cross-functional teams, managing budgets, and creating internal communication content. Requires a Bachelor's degree in a related field and 5 years of experience in marketing, commercial excellence, communication, capability development, or strategic planning.

Leads and manages the DMPK function within respiratory and immunology drug development, providing strategic direction in DMPK approaches for novel therapeutic agents. Collaborates with project teams to support discovery and preclinical to clinical transitions. Shapes the development strategy for R&I programs and acts as a scientific ambassador for DMPK internally and externally. Oversees a team of DMPK experts and ensures DMPK data informs critical decision-making.

Leads Instrumentation and Calibration activities, ensuring compliance with regulatory requirements and industry standards. Manages calibration scheduling, team performance, and troubleshooting efforts for process and utility equipment.

Designs, implements, and evaluates marketing activities for assigned brands. Analyzes market data, identifies growth opportunities, and collaborates with internal and external teams.

Associate Director, GCS Delivery, Solutions Implementation Lead provides technology support and manages clinical technologies for global studies. Leads technology implementation, end-to-end process management, and cross-functional collaboration. Requires a university degree in a relevant field and significant experience in clinical research.

Technical clerk responsible for processing and managing 3D pipe construction documents, creating parts lists, and maintaining data records in IT systems.