Boehringer Ingelheim
(Senior) Patient Safety Physician CRM(m/w/x)
Full-timeOn-siteSenior
Ingelheim am Rhein
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BOBoehringer Ingelheim
(Senior) Patient Safety Physician - Inflammation(m/w/x)
Ingelheim am Rhein
Full-timeOn-siteSenior
Nejo AI Summary
Leading global patient safety and risk management for pharmaceutical compounds in inflammation. Medical Doctor with clinical and PV experience required. Global project collaboration in a research-driven environment.
Requirements
- Medical Doctor with clinical and/or clinical research experience
- PV experience and good understanding of PV regulation in major markets
- Experience in Clinical Development and marketing authorisation submissions (asset)
- Clinical or research experience in disease areas (plus)
- Good interpersonal and communication skills
- Strong ethical sense, quality, and patient safety mindset
- Excellent written and spoken English skills
- Profound experience in PSPV, Risk Management, clinical development, and post-marketing safety (global/corporate level)
- Very good understanding of pharmaceutical industry and pharmacovigilance trends
- Thorough understanding of PV regulation in major markets and compliance
- Project Management competencies
Tasks
- Lead global patient safety and risk management for compounds
- Contribute to global patient safety and risk management for compounds
- Develop patient-centric risk management strategies
- Plan pharmacovigilance activities
- Manage pharmacovigilance activities
- Perform pharmacovigilance activities
- Monitor pharmacovigilance activities
- Set up safety analyses in clinical and safety databases
- Monitor product safety and benefit/risk profile
- Develop product safety and benefit/risk profile
- Manage safety issues
- Develop patient-centric benefit-risk strategies for compounds
- Develop safety-focused post-authorisation studies
- Interpret clinical trial safety data
- Provide medical-scientific input
- Review regulatory documents
- Update senior management on drug safety profile
- Recommend pharmacovigilance and risk management activities
- Chair internal multidisciplinary Asset Benefit Risk Teams
- Participate in internal and external committees
- Stay informed about methodologies, regulations, and trends
- Contribute to pharmacovigilance development
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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BOBoehringer Ingelheim
(Senior) Patient Safety Physician - Inflammation(m/w/x)
Ingelheim am Rhein
Full-timeOn-siteSenior
Nejo AI Summary
Leading global patient safety and risk management for pharmaceutical compounds in inflammation. Medical Doctor with clinical and PV experience required. Global project collaboration in a research-driven environment.
Requirements
- Medical Doctor with clinical and/or clinical research experience
- PV experience and good understanding of PV regulation in major markets
- Experience in Clinical Development and marketing authorisation submissions (asset)
- Clinical or research experience in disease areas (plus)
- Good interpersonal and communication skills
- Strong ethical sense, quality, and patient safety mindset
- Excellent written and spoken English skills
- Profound experience in PSPV, Risk Management, clinical development, and post-marketing safety (global/corporate level)
- Very good understanding of pharmaceutical industry and pharmacovigilance trends
- Thorough understanding of PV regulation in major markets and compliance
- Project Management competencies
Tasks
- Lead global patient safety and risk management for compounds
- Contribute to global patient safety and risk management for compounds
- Develop patient-centric risk management strategies
- Plan pharmacovigilance activities
- Manage pharmacovigilance activities
- Perform pharmacovigilance activities
- Monitor pharmacovigilance activities
- Set up safety analyses in clinical and safety databases
- Monitor product safety and benefit/risk profile
- Develop product safety and benefit/risk profile
- Manage safety issues
- Develop patient-centric benefit-risk strategies for compounds
- Develop safety-focused post-authorisation studies
- Interpret clinical trial safety data
- Provide medical-scientific input
- Review regulatory documents
- Update senior management on drug safety profile
- Recommend pharmacovigilance and risk management activities
- Chair internal multidisciplinary Asset Benefit Risk Teams
- Participate in internal and external committees
- Stay informed about methodologies, regulations, and trends
- Contribute to pharmacovigilance development
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
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