Senior Patient Safety Physician - Cardio Renal Metabolic

Boehringer Ingelheim; Deutschland; Hybrid; EUR 120,000 - 180,000; Full time

Job summary

Boehringer Ingelheim GmbH in Germany is seeking a Senior Patient Safety Physician CRM to lead global patient safety strategy across development and pharmacovigilance, shaping benefit-risk assessments for compounds in development and marketed products. The role requires medical expertise and strategic leadership in a cross-functional environment.

The position offers a hybrid work setup with 2-3 days on site, collaboration with internal teams, regulatory interactions, and DSUR/trial document

Qualifications

• Medical doctor with clinical or research experience in pharmacovigilance.
• Global/corporate PV experience is required.
• Strong understanding of PV regulations in major markets.
• Experience with clinical development and MA submissions is an asset.
• Excellent ethics, quality mindset, and patient safety focus.

Responsibilities

• Lead global patient safety strategy and risk management for assigned products.
• Oversee pharmacovigilance activities from planning to oversight.
• Develop safety analyses using trial and safety databases.
• Prepare regulatory documents (DSURs, risk management plans).
• Represent safety in regulatory interactions and cross-functional committees.

Skills

English proficiency

Project management

Interpersonal communication

Strategic leadership

Education

Medical Doctor

Job description

Senior Patient Safety Physician - Cardio Renal Metabolic

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.

This position can be filled in different countries.

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: [phone] or via mail: [e-mail]

Recruitment process

1. Step 1: Online application
2. Step 2: Virtual meeting starting from October
3. Step 3: On-site interviews beginning of November

Please submit your application documents in English.

Upon applying for this position, you will encounter a query regarding the visibility of your profile - whether it should be confined to the recruiters managing the jobs you apply to, or be accessible to any company recruiter worldwide. Given that the hiring manager is not based in the country you are applying for and the interview process is performed in the hiring manager country, we kindly urge you to opt for "Any company recruiter worldwide". This action will greatly assist us in processing your application in the most efficient manner, while ensuring compliance with the General Data Protection Regulation.