ASSOCIATE VICE PRESIDENT, QUANTITATIVE CLINICAL PHARMACOLOGY

The Associate Vice President, Quantitative Clinical Pharmacology will lead multi-disciplinary project teams through the successful completion of client goals. This role will engage in activities ranging from developing MIDD-based clinical pharmacology strategies for client development programs, serving as an embedded clinical pharmacology representative for clients, supporting clinical pharmacology objectives by providing consultations on study design through the development and evaluation of models, the performance of simulations, and the presentation of results.

Job Responsibilities

• Lead and collaborate with multi-disciplinary teams to implement quantitative clinical pharmacology projects / programs and to provide clinical pharmacology and pharmacometric consultation to other company projects / programs
• Support clinical pharmacology-related components of clinical study protocols, study conduct, data analysis, and report writing independently and with the support of colleagues
• Provide guidance to clients regarding regulatory strategy and participate in regulatory interactions with health authorities on behalf of clients
• Support project teams by providing clinical pharmacology and pharmacometric consulting through advanced PBPK, population PK, PK / PD, and exposure-response modeling and simulation as well as noncompartmental analyses, using GastroPlus, MONOLIXSuite (PKAnalix, MONOLIX, Simulx), NONMEM, R, or other tools
• Apply advanced scientific knowledge and expertise to assigned programs and projects
• Responsible for appropriateness of methods, integrity of data used for analysis, and accuracy of results
• Ensure communication between the company and clients throughout project execution
• Regularly engage with clients regarding the strategic approach, presentation of results, regulatory implications, and messaging of findings
• Initiate and maintain positive, productive, and profitable client relationships
• Prepare final technical reports, synopses, executive summaries, and other regulatory documents, including CTD Section 2.7.2, 2.7.1, Integrated Summary of Efficacy, Integrated Summary of Safety, Briefing Books, Question-and-Response documents, and other documents as needed
• Ensure the provision of advanced literature searches for project / program-related information
• Provide sophisticated written interpretation of material and integrate research findings into project / program methodology and results
• Share findings with internal and external project teams
• Prepare abstracts, presentations, and publication-ready manuscripts
• May supervise junior scientists; provide mentoring and feedback to junior scientists
• Engage in cross-divisional discussions of scientific strategy
• Serve as a subject matter expert resource for the Business Development Team; draft work scopes, strategies, and proposals; develop budgets for new projects
• Integrate knowledge of PBPK, population PK, and PK / PD to provide guidance regarding proposed approaches to addressing drug development and regulatory approval challenges
• Stay current with pharmacometric and clinical pharmacology literature and project / program-related literature
• Expand scientific expertise through attendance and presentation at international, national, and regional scientific conferences, client meetings, and government meetings
• Develop and teach at GastroPlus, MONOLIX, and other workshops and courses
• Other duties as assigned

Qualifications

Education

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