Head of Pharmacology

Job Responsibilities Expand and guide the clinical pharmacology group, including FTEs and external vendors, to address needs in a fast-paced environment. Provide guidance and oversight of clinical pharmacology strategy across the portfolio; advocate for model-informed drug development (MIDD) and build a culture of evidence-based decision-making. Manage the department budget. Collaborate with cross-functional colleagues and leadership to support strategic and scientific planning and execution. Oversee development and implementation of translational strategies. Oversee analysis and interpretation of PK/PD data from clinical studies; collaborate on nonclinical studies using appropriate quantitative methodologies. Oversee clinical pharmacology competitive intelligence analysis and interpretation. Supervise and/or mentor junior scientists; drive process improvement for efficiency and consistency; support employee career development. Interact with external collaborators, board of directors, investors, key opinion leaders, and vendors as appropriate. Author or oversee authorship of regulatory document sections, publications, and represent Clinical Pharmacology in regulatory interactions. Represent Clinical Pharmacology on due diligence teams upon management request. Build Clinical Pharmacology capability in China. Contribute to implementing Artificial Intelligence to support drug development. Other duties as assigned. Qualifications M.D., Ph.D. in Pharmaceutical Sciences/Pharmacokinetics (or related) or PharmD with a Clinical Pharmacology fellowship. 12+ years of industry experience in Clinical Pharmacology in a matrix environment on drug development teams. Proven ability to manage vendor performance and stakeholder relationships while making evidence-based decisions; strong analytical, regulatory, negotiation, and communication skills. Clinical Pharmacology leadership experience in strategic and scientific settings. Cross-functional leadership and supervisory experience. Clinical Pharmacology experience with small molecules and metabolism. In-depth knowledge of global regulatory requirements and guidelines for clinical pharmacology (FDA, EMA, ICH), including interpretation/application and experience with regulatory interactions and filings. Strong interpersonal, communication, negotiation, and cross-cultural collaboration skills; ability to present complex concepts clearly and make sound decisions under pressure. Travel Required Occasional travel to conferences and company-related activities (including travel to China). #J-18808-Ljbffr