(Senior) Patient Safety Physician CRM

Position

The Position

Overview

Are you a Medical Doctor passionate about patient health and safety? Boehringer Ingelheim’s TA CRM Team seeks experienced (Senior) Patient Safety Physicians to contribute to late‑stage clinical development or post‑marketing drug safety, particularly in cardiovascular, renal, hepatic, and/or metabolic diseases.

Responsibilities

• Lead or contribute to integrated Patient Safety and Pharmacovigilance (PSPV) activities for compounds in clinical development or in the market.
• Design and implement strategies to generate appropriate safety evidence.
• Develop proactive, patient‑centric risk minimisation strategies for assigned compounds.
• Plan, manage, and monitor PV activities, 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.
• Collaborate with Clinical Development and Global Patient Engagement to develop patient‑centric benefit‑risk profile assessment strategies for developmental compounds.
• Work with Global Epidemiology and Medical Affairs to develop safety‑focused post‑authorization studies.
• Interpret clinical trial safety data for clinical trial reports and submission documents.
• Review and provide medical‑scientific input to regulatory documents (IBs, PSURs, DSURs, RMPs, Clinical Overview Statements).
• Update senior management on the assigned drug’s safety profile and recommend PV/RM activities to BI decision‑making committees.

Senior Position Additional Responsibilities

• Chair Boehringer Ingelheim internal multidisciplinary Asset Benefit Risk Teams.
• Represent PSPV in internal and external committees.
• Contribute 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.
• Pharmacovigilance experience and good understanding of PV regulations in major markets.
• Experience in clinical development and submissions for marketing authorization is an asset.
• Clinical or research experience in cardio‑renal‑metabolism areas is 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.

Senior Position 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.
• Very good and broad understanding of the pharmaceutical industry, 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.

Contact

Contact our HR Direct Team: Tel: +49 (0) ‑3330 or email: ‑ingelheim.com.

Recruitment Process

• Step 1: Online application – application period extends until January 15th, 2026. Applications up to January 5th, 2026 are guaranteed consideration.
• Step 2: Virtual meeting – beginning mid‑January 2026.
• Step 3: On‑site interviews – starting the second half of January 2026.

About the Company

Boehringer Ingelheim is committed to developing innovative therapies that transform lives. We value diversity, authenticity, and bold innovation, providing a respectful and friendly environment where everyone is valued and welcomed. For more information, visit