Study Physician (m/f/d)
Boehringer Ingelheim RCV GmbH & Co KGOur Company
At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.
The position
The Study Physician is a global role in Clinical Development Therapeutic Area at Boehringer Ingelheim. Study Physician is responsible for the medical content and medical oversight in the allocated clinical trials as a qualified and clinically experienced physician. Medical input for the clinical trial and being involved in the project/asset team by provision of state-of-the-art medical expertise with the aim to execute medical oversight and support in management of clinical trials during the preparation, conduct, and reporting phase of clinical trials. This role is critical within Clinical Development Therapeutic Area. Study Physician is a core member of the Trial Team and member of the Evidence Network for the asset.
Tasks & responsibilities
- Responsible for end-to-end medical support throughout the entire study lifecycle, from TDO kick-off to the Clinical Trial Report
- Ensures high-quality medical content of the Clinical Trial Protocol, collaborating closely with CTL, CPL, Patient Safety, and other cross-functional stakeholders
- Develops the Clinical Quality Monitoring Plan, conducts ongoing medical data review, supports risk-based quality management, and defines key protocol deviations
- Provides medical input for investigator and study team trainings, eCRF design, automated data checks, ICF, lab alerts, feasibility, and recruitment activities; contributes to regulatory and ethics responses
- Acts as the primary contact for medical questions from Investigators and contributes to adjudication and Data Monitoring Committee processes
Requirements
- Medical degree (MD) with clinical training and at least 4 years of active clinical practice; a specialization in Internal Medicine or General Practice is an advantage
- Professional experience in the pharmaceutical industry or a CRO, ideally in medical or project-related roles
- Solid understanding of ICH-GCP regulations, clinical research processes and relevant regulatory guidance
- Strong analytical and communication skills, structured working style and ability to collaborate effectively in an international environment
- Proficiency in medical data review/analysis and fluency in English (written and spoken)
Your Benefits
- Flexible working time models: home office and flexible working hours, depending on department and position – many things are possible with us.
- Additional days off (“bridge-days”): more free time through additional days off to bridge single working days between bank holidays and the weekend – without having to use vacation days.
- Canteen & Cafeteria: whether it's coffee and croissant for breakfast, various lunch menus or snacks in between – our subsidized staff restaurant & cafeteria has something for every taste including vegetarian and vegan options.
- Learning & development: diverse training and development opportunities for your personal and professional growth. Because: you never stop learning.
- Health promotion: health is important to us – that's why we offer different programs to promote physical and mental health.
- Public transport ticket: we encourage our employees to use public transport on their daily way to work. Costs for public transport? We cover them!
The remuneration for this position starts at EUR 108.000 gross annual target salary per year (full time). The actual salary package depends on professional experience and qualifications. We will be happy to discuss further details in person.
We are looking forward to receiving your application online!
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Do you have any additional questions about the position? Your HR Recruiting Manager for this position is Martina Prenn.
On our career site you will find further information about Boehringer Ingelheim as an employer as well as information about the application process and our different departments.
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