About this role
The Position Lead the Future of Medicine – as Senior Patient Safety Physician CRM Lead global patient safety strategy and shape the development of innovative medicines. As a Senior Patient Safety Physician, you will provide medical and strategic leadership across clinical development and pharmacovigilance activities, driving benefit-risk assessments and patient safety strategies for compounds in development and marketed products. Working within a global, cross-functional environment, you will play a key role in enabling informed development decisions and bringing meaningful therapeutic innovations to patients worldwide.
Join us in shaping the future of medicine – apply now! This position can be filled in Ingelheim or Biberach This position has a hybrid setup with approximately 2-3 days per week on site. Tasks & responsibilities As part of your role, you will design and implement proactive, patient-centric risk management strategies for assigned compounds, ensuring alignment with global safety standards.
Leading all pharmacovigilance activities for your designated products, you will be responsible for planning, execution, and continuous oversight up to POC. To support effective safety monitoring, you will establish and refine safety analyses within clinical trial and safety databases. A key aspect of your work involves continuously evaluating and enhancing the benefit-risk profile of your products by integrating clinical data and patient insights.
You will engage in close collaboration with internal teams and external stakeholders to address safety concerns and implement appropriate risk mitigation strategies. Your medical-scientific expertise will be essential in preparing regulatory documents such as DSURs, and trial related documents such as investigator’s brochure, clinical trial protocols, clinical reports ensuring accuracy and compliance. In your senior capacity, you will chair the multidisciplinary Asset Benefit-Risk Team and represent Experimental Medicine Patient Safety in strategic committees and regulatory interactions.
Requirements Medical Doctor with long-standing clinical or research experience, experience in CRM (cardio renal metabolic) therapeutic area would be an asset. Profound experience in pharmacovigilance and Risk Management in a pharmaceutical company on a global / corporate level, including clinical development and post-marketing safety. Thorough understanding of PV regulation in major markets and respective need for compliance Experience in clinical development and submissions for marketing authorization would be an asset Very good and broad understanding of the pharmaceutical industry, and the future trends and developments including pharmacovigilance Strong ethical sense combined with quality and patient safety mindset Profund Project Management competencies with good interpersonal and communication skills Excellent English skills, both written and spoken As part of our commitment to transparency and fairness, salary information will be shared during the recruitment process.
We also offer a comprehensive benefits and wellbeing package. Applications from persons with severe disabilities are warmly welcomed. In cases of equal qualifications, such applicants will be given preferential consideration in the selection process.
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 via mail: hr.de@boehringer-ingelheim.com Recruitment process: Step 1: Online application Step 2: Virtual meeting starting from October Step 3: On-site interviews beginning of November Please submit your application documents in English.