Head, Clinical Pharmacology

il y a 1 semaine


Paris, France Ipsen Temps plein

Head, Clinical Pharmacology Location: Paris, France or London, UK or Cambridge, US. The Senior Leader will report to the VP, Head of Clinical Pharmacology, DMPK & Pharmacometrics and work across R&D, Early Development, Clinical Operations, Regulatory Affairs, and external partners. Role Summary The Head leads a team of Clinical Pharmacology leads, provides strategic direction, and delivers all clinical pharmacology studies across the IPSEN portfolio, including small molecules, peptides, biologics (mAbs, ADCs, proteins), and due‑diligence for external assets. The role drives innovative methodologies to accelerate drug development, mentors talent, and ensures seamless integration of clinical pharmacology insights into asset development and lifecycle management. Key Responsibilities Lead the Clinical Pharmacology Group and act as Clinical Pharmacology lead on projects, ensuring alignment with R&D objectives. Recruit, mentor, and develop a high-performing team of Clinical Pharmacologists. Define and implement best practices for study design and execution across modalities. Provide expert input into first‑in‑human strategy and study design, integrating translational insights and model‑informed drug development. Serve as the Clinical Pharmacology representative on cross‑functional project teams, contributing to early development strategy. Collaborate with internal and external stakeholders on in‑licensing opportunities and external assets. Oversee planning and delivery of studies such as SAD, MAD, DDI, HMB, TQT, and Food Effects, ensuring scientific rigor, operational excellence, and regulatory compliance. Manage EHS responsibilities, enforce regulations, participate in safety visits, and ensure mandatory training completion. Drive the strategic vision for clinical pharmacology, cultivate innovation, and foster strong partnerships across departments and external collaborators. Knowledge & Experience (Essential) 10+ years in pharmaceutical/biotech with proven leadership in cross‑functional environments. Hands‑on experience with SAD, MAD, DDI, HMB, TQT, BE, and Food Effect studies. Demonstrated success managing multiple Phase I studies concurrently. Strong understanding of clinical trial management, data management, and the end‑to‑end drug development process. Operational excellence in project management, planning, prioritization, and problem‑solving. Excellent interpersonal skills with a proven ability to build relationships and influence stakeholders. Exceptional communication, attention to detail, and cultural sensitivity. Leadership and management experience with a recognized leadership profile. Strategic vision with a big‑picture perspective while managing critical details. Professional representation with integrity and professionalism. Self‑directed, flexible, solution‑oriented, and positivity. Passion for continuous learning and development of self and others. Education / Certifications (Essential) MD, PhD, or PharmD with a minimum of 10 years in Clinical Pharmacology & DMPK in pharma and/or biotech. Languages (Essential) English: Excellent written, verbal, and interpersonal communication skills. Other Information Seniority level: Not Applicable Employment type: Full‑time Job function: Other Industries: Pharmaceutical Manufacturing #J-18808-Ljbffr


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