
10,000+ employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Boehringer Ingelheim is a global, research-driven, family-owned pharmaceutical company headquartered in Germany that discovers, develops, manufactures, and markets prescription medicines, biopharmaceuticals, vaccines, and animal health products. The company focuses on therapeutic areas including respiratory, cardiovascular, metabolic, oncology, immunology, and zoonotic diseases, and invests heavily in R&D and biotechnology to advance drug discovery and development. It operates worldwide across both human pharmaceuticals and animal health markets, partnering with academic institutions and biotech firms to translate scientific research into therapies.
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10,000+ employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Boehringer Ingelheim is a global, research-driven, family-owned pharmaceutical company headquartered in Germany that discovers, develops, manufactures, and markets prescription medicines, biopharmaceuticals, vaccines, and animal health products. The company focuses on therapeutic areas including respiratory, cardiovascular, metabolic, oncology, immunology, and zoonotic diseases, and invests heavily in R&D and biotechnology to advance drug discovery and development. It operates worldwide across both human pharmaceuticals and animal health markets, partnering with academic institutions and biotech firms to translate scientific research into therapies.
• Provide end-to-end medical support throughout the entire study lifecycle, from Trial Design Outline kick-off to the Clinical Trial Report • Ensure high-quality medical content of the Clinical Trial Protocol • Contribute to core trial documents in collaboration with the Clinical Trial Leader, Clinical Program Lead, Patient Safety Physician, and cross-functional stakeholders • Contribute to trial risk-based quality management from a medical perspective • Define medically relevant critical data and processes, related risks, and mitigation and monitoring strategies • Take medical responsibility for agile and adaptive medical data review • Develop the Clinical Quality Monitoring Plan and define important protocol deviations • Provide medical training for investigators and the study team • Contribute to eCRF design, automated data checks, ICF, lab alerts, recruitment and retention activities, and regulatory and ethics responses • Answer medical questions from investigators • Contribute to adjudication and Data Monitoring Committee processes • Serve as a core member of the Trial Team and a member of the Evidence Network for the asset
• Physician (MD), ideally with medical thesis • Trained in a clinical setting • Minimum of four (4) years of active clinical practice experience • Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine is desirable • Experience specifically in Inflammation Clinical Development is preferred • Experience in pharma industry or CRO in medical or project management functions, ideally in Clinical Development, is desirable • Ability to communicate directly and concisely while collaborating with key stakeholders • Pronounced presentation and training skills • Capability to work proactively and with team spirit in an international environment and team • Pronounced analytical skills and systematic, well-structured working style • Ability to use digital technologies to access information, be creative, innovate, solve problems, communicate, navigate, learn, and apply in a digital environment
• Flexible working time models: home office and flexible working hours, depending on department and position • Additional days off (“bridge-days”) • Subsidized staff restaurant & cafeteria, including vegetarian and vegan options • Diverse training and development opportunities • Health promotion programs for physical and mental health • Public transport ticket costs covered
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