(Senior) Clinical Program Leader CRM
The Position
In your new role, you are responsible for the design and preparation of late clinical development plans in Clinical Development Cardiorenal & Metabolism, and submission documents to prepare assets in one or more of the following areas: Obesity, Metabolic Dysfunction Associated Steatohepatitis (MASH), Cardiovascular indications, Stroke, and/or chronic kidney disease (CKD) for worldwide registration.
Tasks & responsibilities
- In alignment with the clinical development plans and as agreed with regulatory authorities (e.g. EMA and FDA), you conduct scientifically and clinically rigorous trials, contribute to relevant investigator`s brochures and develop clinical trial protocols, amendments, modifications of clinical investigational plans, clinical trial reports and scientific publications.
- You are responsible for trial start-up, trial conduct, data read out and submission to achieve registration for novel assets.
- Furthermore, you work in close collaboration with Early Clinical Development team members, Medical Affairs and Market Access to ensure smooth transition of assets across various development phases.
- With your expertise, you ensure a good understanding of the relevant customer groups for Obesity, MASH, Cardiology, Stroke and/or CKD (health authorities, key external experts, associations, patient groups, payers, etc.).
- You act as a decision maker in trial-related internal & external committee meetings, as delegated by the Head of Clinical Development or Clinical Development Leader.
- Furthermore, you are an externally recognized expert in the field and represent Boehringer Ingelheim to experts, regulatory authorities and organizations.
- In cooperation with the Head of Clinical Development or Clinical Development Leader, you exert medical and scientific leadership for cardiovascular indications within Clinical Development CRM.
Requirements
- MD with initial clinical and scientific experience in Medicine, preferably Endocrinology/Metabolism, Gastroenterology & Hepatology, Cardiology, Nephrology, Neurology, or Internal Medicine; Clinical / Pharma experience in the US is a plus
- Some years of experience in clinical drug development within pharma industry, or comparable clinical development experience in an academic setting
- Regulatory knowledge and experience with various agencies like FDA and EMA
- Excellent leadership communication (oral and written) as well as negotiation and influencing skills
- Ability to act with grace and resilience under pressure as well as excellent presentation, training and facilitation skills
Additional Requirements for the Senior Role:
- MD with multiple years of clinical and scientific experience in Medicine, Endocrinology/Metabolism, Gastroenterology & Hepatology, Cardiology, Neurology, Nephrology, or Internal Medicine; Clinical / Pharma experience in the US is a plus
- Long-term experience in Clinical Drug Development in pharma industry and/or academia, preferably in an international role
- In-depth regulatory expertise with prior successful interactions with various agencies like FDA and EMA
- Excellent leadership communication (oral and written) as well as negotiation and influencing skills
- Ability to act with grace and resilience under pressure as well as excellent presentation, training and facilitation skills
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: hr.de@boehringer-ingelheim.com
The job posting is presumably online until January 31st, 2026. We reserve the right to take the posting offline beforehand.