Senior Patient Safety Physician

The PositionLead the Future of Medicine – as Senior Patient Safety Physician CRMLead 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 BiberachThis position has a hybrid setup with approximately 2-3 days per week on site.Tasks & responsibilitiesAs 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.RequirementsMedical 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 complianceExperience in clinical development and submissions for marketing authorization would be an assetVery good and broad understanding of the pharmaceutical industry, and the future trends and developments including pharmacovigilanceStrong ethical sense combined with quality and patient safety mindsetProfund Project Management competencies with good interpersonal and communication skillsExcellent English skills, both written and spokenAs 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) or via mail: process:Step 1: Online applicationStep 2: Virtual meeting starting from OctoberStep 3: On-site interviews beginning of NovemberPlease submit your application documents in English.