Boehringer Ingelheim

Senior Clinical Program Leader - Obesity & Liver

Stellenbeschreibung:

Overview

In this role, you drive early-phase obesity and liver programs from strategy through execution, leading cross-functional teams to advance therapies. You’ll influence regulatory strategy and contribute to Medical Affairs plans, shaping evidence generation and decision-making across development. You will mentor other clinical leads and act as a delegate for the Clinical Development Lead when needed. This position offers the chance to impact global patient care through scientific leadership and collaboration.

Verantwortungsbereiche
  • Design and oversee Phase I–II clinical development plans for obesity and liver indications
  • Lead cross-functional teams across trial operations, biostatistics, biomarkers, and patient safety to ensure high-quality execution
  • Manage setup, conduct, and data readout of trials in collaboration with the Clinical Trial Lead
  • Provide input to regulatory strategy and contribute to briefing documents and regulatory responses
  • Contribute to Medical Affairs strategy and deliverables (e.g., Integrated Evidence Plan) with Medical Advisors
  • Evaluate external opportunities to strengthen the pipeline and inform decision-making
  • Supervise and mentor other Clinical Program Leads within the program/asset and serve as a delegate for the Clinical Development Lead
Zentrale Anforderungen
  • MD degree with extensive clinical and scientific experience in metabolic diseases, cardiovascular, renal, or internal medicine
  • Long-term experience in clinical drug development in the pharmaceutical industry or equivalent academic clinical research
  • Strong leadership and ability to motivate cross-functional teams
  • Proven ability to influence and collaborate with diverse stakeholders
  • Skilled in presenting scientific content and facilitating cross-functional discussions
  • High initiative, strategic thinking, and team orientation
  • Excellent English communication skills (written and verbal)
  • leadership
  • cross-functional collaboration
  • communication
  • clinical drug development
  • regulatory strategy input
  • trial design and execution (Phase I–II)
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Stelleninformationen

  • Veröffentlichungsdatum:

    14 Sep 2026
  • Standort:

    Berlin

    Einsatzort:

    Mecklenburg-Vorpommern und Nord-Brandenburg
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

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