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Boehringer Ingelheim

Senior Clinical Program Lead

Boehringer Ingelheim

(Senior) Clinical Program Lead overseeing clinical trials for obesity and liver diseases. Guiding teams and ensuring high-quality execution in a newly established Global Clinical Development organization.

Posted 7/11/2026full-time🇩🇪 GermanySeniorWebsite

About the role

Key responsibilities & impact
  • Design and prepare clinical development plans, focusing on Phase II and III in obesity and liver diseases.
  • Guide cross-functional teams, including experts from clinical trial operations, biostatistics, biomarkers, and patient safety, to ensure high-quality execution as the clinical lead.
  • Oversee the setup, conduct, and data readout of clinical trials in collaboration with the Clinical Trial Lead, ensuring timelines, quality, and ethical standards are met.
  • Provide input to regulatory strategy and clinical components of briefing documents, presentations, and responses to questions.
  • Contribute to the Medical Affairs strategy and deliverables, including key documents such as the Integrated Evidence Plan, in collaboration with Medical Advisor(s) and the Medical Affairs Lead.
  • Leverage clinical expertise to evaluate external opportunities and support decisions that strengthen the pipeline.
  • Supervise and mentor other Clinical Program Leads within the assigned program/asset.
  • Act as a delegate for the Clinical Development Lead in designated tasks and responsibilities, as required.

Requirements

What you’ll need
  • MD degree with several years of clinical and scientific experience in metabolic diseases, cardiovascular, renal or internal medicine
  • Few years of experience in clinical drug development within the pharmaceutical industry or equivalent experience in academic clinical research
  • Ability to influence and collaborate effectively across diverse stakeholder groups
  • Skilled in presenting scientific content and facilitating cross-functional discussions
  • High level of initiative, strategic thinking, and team orientation
  • Excellent communication skills in English, both written and verbal
  • MD degree with long-standing clinical and scientific experience in metabolic diseases, cardiovascular, renal or internal medicine
  • Long term experience in clinical drug development within the pharmaceutical industry or equivalent experience in academic clinical research
  • Strong leadership skills with the ability to lead and motivate cross-functional teams

Benefits

Comp & perks
  • Comprehensive benefits and wellbeing package

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Clinical Development PlansClinical Trial OperationsBiostatisticsData ReadoutRegulatory StrategyMedical Affairs StrategyIntegrated Evidence PlanClinical ResearchPatient SafetyCross-Functional Collaboration
Soft Skills
Excellent Communication SkillsInfluencing SkillsTeam OrientationInitiativeFacilitating Discussions