The Position
Lead the Future of Medicine – as Scientific Monitor
To ensure the fastest and most focused path from strategy to patients, we are evolving our OneHP organization. Together, we are simplifying our structures, strengthening the accountability of Therapeutic Areas, and creating clear interfaces between Innovation and Business. This ensures that our assets are efficiently transformed into successful brands – with the ultimate goal of delivering lasting value to patients around the world. Therefore, we are looking for a Scientific Monitor to help shape our newly established Global Experimental Medicine organization. Your mission: elevate early clinical development, accelerate the path to Proof of Concept, and pave the way for breakthrough therapies.
Now is the time to act – to strengthen our organization, empower our teams, and fulfill our responsibility to patients worldwide.
Join us in shaping the future of medicine – apply now!
This position has a hybrid setup with approximately 1-2 days per week on site.
This position is part time eligible with min. 80%.
Tasks & responsibilities
- In your new role, you will oversee external biomarker lab activities to ensure that timelines and agreed services are conducted.
- You will work together with Biomarker Leads, CDx Leads, clinical trial leads, data managers, Clinical Biosample Operations, and other relevant functions to deliver data on time and in the desired quality.
- Furthermore, you will collaborate with international external partners and vendors to get clinical studies and research collaborations set up and running.
- Moreover, you will chair international meetings and train relevant interface parties.
- You will collaborate proactively and decisively within the international interdisciplinary team to achieve optimal outcomes for the clinical trial. Finally, you will approve the usage of human biospecimens based on Boehringer internal regulations within ExpMed TA Oncology.
Requirements
- Completed Bachelor’s degree in a medical-scientific subject or equivalent education with several years of working experience in laboratory analytics for human samples (preferably in Genomics) or other experience in clinical studies
- Experience in Oncology trial set-up, contracting of CROs/universities, CDx developments and as Human Biospecimen Acquisition Manager
- GCP knowledge including experience in inspections, advanced skills in MS Office and Veeva applications with expertise in CDx development processes and regulations
- Independent, collaborative and structured work style with outstanding interpersonal and communication skills
- Strong Teamplayer with innovative mindset to work effectively in a fast-changing environment, capable of working in multi-disciplinary and global teams Excellent English, both spoken and written
Ready to contact us?
If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: +49 (0) 6132 77-3330 or via mail: [email protected]
Recruitment process:
Step 1: Step 1: Online application - The job posting is presumably online until "August 25th, 2025".
Step 2: Virtual meeting beginning of September
Step 3: On-site interviews starting in mid of September
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