265 English-speaking jobs in Schleswig-Holstein

Designs and implements strategic brand initiatives for the rare disease sector. Develops local brand strategies, conducts market analysis, and manages marketing campaigns. Collaborates with cross-functional teams to ensure unified brand messaging and successful strategy execution.

Leads medical strategy and field excellence for Cardiovascular, Renal and Metabolism portfolios. Guides a team of Medical Science Liaisons and Therapeutic Area partners to deliver medical initiatives. Integrates scientific knowledge and trends to shape national strategies and cross-therapeutic area priorities.

Develop, test, and implement FTE demand algorithms using PLANIT for BioPharma ClinOps. Collaborate with stakeholders to align with organizational productivity initiatives. Manage the BAU process for ongoing review and refinement of algorithms.

Global Safety Program Lead responsible for the overall scientific and clinical safety content for assigned assets. Accountable for safety strategy, deliverables, and compliance with PV regulations. Leads safety teams, provides strategic safety knowledge, and represents Global Patient Safety at governance forums. Requires a medical degree or equivalent and 5+ years of relevant clinical, safety, and risk management experience.

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.

Provides administrative support to the Oncology department. Duties include document archiving, communication management, meeting coordination, procurement, and workflow management. Requires a university degree, advanced English proficiency, and experience in a similar role.

Leads regulatory affairs for assigned pharmaceutical franchises from clinical development to life cycle maintenance. Develops regulatory strategies, ensures compliance, and collaborates cross-functionally. Requires a pharmacy graduate with people management experience and expertise in Indian regulations.

Leads medical strategy for new and existing products, providing clinical development expertise, RWD/RWE proficiency, and market access knowledge. Collaborates cross-functionally and externally to shape launch strategies and drive commercialization. Requires a medical degree and experience in clinical practice, medical affairs, or clinical operations.

The Global Safety Head is responsible for all safety aspects of assigned assets, including strategy, risk management, and communication. Leads safety strategy development and execution, ensuring compliance with regulations and AZ policies. Manages a team of Global Safety Program Leaders and provides safety input into project strategy across the asset lifecycle. Requires a medical degree or equivalent, 8+ years of relevant experience, and direct experience with global regulatory filings.

The Diagnostic Manager develops and implements diagnostic strategies for assigned therapeutic areas, ensuring timely and high-quality testing solutions. This role involves building partnerships with oncology stakeholders, monitoring project progress, and collaborating with medical and commercial teams.

Leads clinical safety strategy, shaping risk management, safety surveillance, and regulatory outcomes for a global development portfolio. Provides medical input to ensure risk-minimization strategies are implemented appropriately and contributes to global regulatory submissions. Requires a medical degree or equivalent experience and at least 2 years of clinical experience post-registration.

Leads the strategy and execution of early process development and analytical methods for novel in vivo lentiviral vectors. Collaborates with discovery teams and cross-functional groups to inform late process design, characterization, and fit-for-purpose analytics.

Senior Medical Director will lead early phase I-II global clinical trials for kidney disease compounds. Responsibilities include clinical strategy, protocol design, study conduct, data interpretation, and reporting. Requires MD, MBBS or MD/PhD with clinical or research expertise in kidney disease treatment and experience in early clinical trials.

Designs, implements, and evaluates marketing activities for assigned brands, including distribution channel solutions. Analyzes market data, identifies growth opportunities, and collaborates with internal and external teams to execute marketing plans.

Senior Analyst - Website Delivery will drive the implementation of OneAZ product features into market websites. Responsibilities include participating in governance meetings, acting as a technical point of contact, ensuring timely training of assembly team members, and collaborating with developers, designers, and product owners. The role requires 10+ years of experience in web development and testing, deep technical competence in AEM, HTML5, CSS3 & JS, and expertise in website governance & operation.

As a Medical Scientific Liaison, you will build and maintain relationships with scientific leaders and stakeholders, develop scientific programs, and act as a scientific expert in priority disease areas.

Senior Statistician II provides statistical expertise for complex clinical program design, analysis, and interpretation. Leads statistical analysis plan development and guides less experienced statisticians. Contributes to regulatory submissions and identifies opportunities for process improvement. Requires a Master's or PhD in Statistics or related field and 3+ years of pharmaceutical development experience.

Regulatory Affairs Specialist will obtain and maintain regulatory approval for product registration in Taiwan, ensuring compliance with Good Regulatory Practice (GRP). Responsibilities include preparing registration documents, maintaining licenses, responding to regulatory inquiries, and collaborating with internal and external stakeholders.

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.

Leads a group of submissions or programs, overseeing communication strategy and driving the use of drug and disease-specific knowledge. Develops and optimizes communication strategies, content, and processes across multiple programs or submissions. Authors and reviews key submission documents, ensuring consistency of messaging. Represents Clinical Regulatory Writing on improvement workstreams and external activities. Supports recruitment and onboarding activities. Minimum Master's degree in a scientific discipline required, PhD preferred. Proficiency in authoring/editing and managing clinical regulatory documents and submissions. Thorough understanding of oncology drug development and knowledge of oncology endpoints required. Experience in program management and stakeholder communication.