The Position Are you a Medical Doctor who is passionate about patient health and safety? If yes, we have an exciting opportunity for you! Our dedicated TA CRM Team is seeking experienced (Senior) Patient Safety Physicians to join us on our journey. You'll have the chance to work on a variety of products, either in late-stage clinical development or post-marketing drug safety. We're particularly interested in physicians with expertise in cardiovascular, renal, hepatic, and/or metabolic diseases. Ready to make a real difference in patient safety? We look forward to your application! Tasks & Responsibilities In this role as a (Senior) Associate Director / (Senior) Patient Safety Physician for Cardio-Renal-Metabolism, you will lead or contribute to integrated Patient Safety and Pharmacovigilance (PSPV) activities for compounds in clinical development or in the market.In more detail, your tasks may include: Designing and implementing strategies to generate appropriate safety evidence Developing and contributing to proactive, patient-centric risk minimization strategies for assigned compounds Planning, managing, and monitoring PV activities for assigned drugs, including: Setting up safety analyses in clinical trial and safety databases for monitoring Continuously monitoring and further developing the product safety and benefit/risk profile Managing safety signals Collaborating with various departments, including Clinical Development and Global Patient Engagement, to develop patient-centric benefit-risk profile assessment strategies for developmental compounds Working with Global Epidemiology and Medical Affairs to develop safety-focused post-authorization studies Interpreting clinical trial safety data for clinical trial reports and submission documents Reviewing and providing medical-scientific input to regulatory documents (e.g., IBs, PSURs, DSURs, RMPs, Clinical Overview Statements) Updating senior management on the assigned drug's safety profile and recommending PV/RM activities to BI decision-making committees For the Senior position, additional responsibilities include: Chairing Boehringer Ingelheim internal multidisciplinary Asset Benefit Risk Teams Representing PSPV in internal and external committees Contributing to the further development of PSPV within BI by staying abreast of state-of-the-art methodology and technology, changes in the regulatory environment, and developments and trends in the healthcare system and society Requirements Medical Doctor with clinical and/or clinical research experience PV experience and good understanding of PV regulations in major markets Experience in clinical development and submissions for marketing authorization would be an asset Clinical or research experience in the field of cardio-renal-metabolism areas would be a plus Strong interpersonal and communication skills A strong ethical sense combined with quality and patient safety mindset Excellent English skills, both written and spoken For the Senior position, you need to meet the additional requirements: Extensive experience in PSPV and Risk Management in a pharmaceutical company on a global/corporate level, including clinical development and post-marketing safety A very good and broad understanding of the pharmaceutical industry, as well as future trends and developments in pharmacovigilance Thorough understanding of PV regulations in major markets and the respective need for compliance Project management and leadership competencies Ready to contact us? If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: 49 (0) 6132 77-3330 or per mail: hr.de@boehringer-ingelheim.com Recruitment process: Step 1: Online application - The job posting is presumably online until January 15th, 2026. We reserve the right to take the posting offline beforehand. Applications up to January 5th, 2026 are guaranteed to be considered. Step 2: Virtual meeting beginning till mid of January 2026 Step 3: On-site interviews starting the second half of January 2026 Unser Unternehmen Bei Boehringer Ingelheim entwickeln wir bahnbrechende Therapien, die das Leben von Mensch und Tier verbessern. Als 1885 gegründetes und seitdem im Familienbesitz befindliches Unternehmen nehmen wir eine langfristige Perspektive ein. Mit 52.000 Mitarbeitenden weltweit setzen wir unsere Ziele um und fördern dabei eine vielfältige, gemeinschaftliche und inklusive Unternehmenskultur. Wir sind überzeugt: Mit talentierten und ambitionierten Mitarbeitenden und ihrer Leidenschaft für Innovationen heben wir die Grenzen des Erreichbaren immer wieder auf. Warum Boehringer Ingelheim? Bei uns können Sie wachsen, zusammenarbeiten, innovativ sein und Leben verbessern. Wir bieten Ihnen herausfordernde Tätigkeiten in einem respektvollen und kollegialen globalen Arbeitsumfeld mit einer Vielzahl von auf Innovation ausgerichteten Denkweisen und Methoden. Darüber hinaus sind für uns Qualifizierung und Entwicklung für alle Mitarbeitenden von zentraler Bedeutung, denn Ihr Wachstum ist unser Wachstum. Boehringer Ingelheim ist ein globaler Arbeitgeber, der sich für Chancengleichheit einsetzt, und ist stolz auf seine vielfältige und inklusive Kultur. Wir begrüßen die Vielfalt von Perspektiven und streben nach einem inklusiven Umfeld, wovon unsere Mitarbeiter*innen, Patienten*innen und Communitys profitieren. Sie möchten mehr erfahren? Dann lesen Sie hier weiter https://www.boehringer-ingelheim.com