Strategic Leader, Obesity & Liver Clinical Programs

Boehringer Ingelheim GmbH; Ridgefield (CT); Ibrido; USD 250.000 - 394.000; Tempo pieno

Descrizione del lavoro

Boehringer Ingelheim is seeking a Director, Senior Clinical Program Leader to drive clinical development in Obesity and Liver. You will oversee medico-scientific strategy, lead cross-functional teams, and shape evidence generation to accelerate regulatory approvals and patient access.

This role requires MD or PhD with extensive drug-development experience and a global, matrix-driven leadership style. Based in the United States, the position emphasizes ethical leadership, collaboration with

Competenze

• MD (specialist in respective TA) with extensive experience across all stages of clinical drug development.
• PhD with ten-plus (10+) years’ experience in respective TA and extensive experience across all stages of clinical drug development.
• Ability to evaluate key study concepts including background, sample size, statistics, design, timing, feasibility and budgeting.
• Strong leadership to drive complex, high-priority projects in global matrix teams.
• Excellent communications, influencing, presentation and training skills.

Mansioni

• Design and oversee clinical development plans focusing on Phase I and II in Obesity & Liver indications.
• Accountable for medical strategy to drive key clinical program deliverables throughout development.
• Lead cross-functional evidence teams and present updates to governance committees and external bodies.
• Ensure integration of regional input and alignment of strategy with operational excellence.
• Author Investigator Brochures, Clinical Development Plans, and core regulatory documents.

Formazione

MD specialist in respective TA

PhD with 10+ years experience in respective TA

Descrizione del lavoro

Boehringer Ingelheim is seeking a Director, Senior Clinical Program Leader to drive clinical development in Obesity and Liver. You will oversee medico-scientific strategy, lead cross-functional teams, and shape evidence generation to accelerate regulatory approvals and patient access.

This role requires MD or PhD with extensive drug-development experience and a global, matrix-driven leadership style. Based in the United States, the position emphasizes ethical leadership, collaboration with