(Senior) Clinical Program Lead

Boehringer Ingelheim; Ingelheim am Rhein; Vor Ort; EUR 80.000 - 100.000; Vollzeit

Benefits dieser Stelle

Comprehensive benefits and wellbeing package

Preferential consideration for applicants with disabilities

Zusammenfassung

Boehringer Ingelheim in Ingelheim am Rhein is looking for a Senior Clinical Program Lead to design and oversee clinical development plans targeting obesity and liver diseases. This role involves collaborating with cross-functional teams and ensuring high-quality execution of clinical trials.

The ideal candidate will have an MD degree and extensive clinical experience in metabolic diseases, as well as strong leadership skills to drive project success in a collaborative environment.

Qualifikationen

• Several years of clinical experience in metabolic diseases or internal medicine.
• Experience in clinical drug development within the pharmaceutical industry.
• Ability to present scientific content effectively.

Aufgaben

• Design clinical development plans for Phase II and III in obesity and liver diseases.
• Guide cross-functional teams to ensure high-quality execution.
• Oversee clinical trials ensuring timelines and ethical standards.

Kenntnisse

Clinical experience in metabolic diseases

Excellent communication skills

Ability to influence and collaborate

Leadership skills

Ausbildung

MD degree

Jobbeschreibung

Tasks & Responsibilities

• 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

Additional tasks for the Senior Role

• 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

• 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

Additional requirements for the Senior Role

• 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

We also offer a comprehensive benefits and wellbeing package.

Applications from persons with severe disabilities are warmly welcomed. In cases of equal qualifications, such applicants will be given preferential consideration in the selection process.