Associate Director, Quantitative Clinical Pharmacology

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Full Time Professional US 1 Attachments

Salary Range: $ To $ Annually

Simulations Plus stands as a global leader in model-informed and AI-accelerated drug development. We create value for our clients by accelerating the discovery, development, and commercialization of pharmaceuticals and other products through innovative science-based software and consulting solutions.

Leadership truly cares about maintaining a positive culture and employee well-being. We offer fully remote work, flexible schedules, and generous vacation policy along with affordable health coverage, annual bonus, and more! Check out how much our employees love working here:  .

The Associate Director, Quantitative Clinical Pharmacology will lead multi-disciplinary project teams through the successful completion of client goals. This role will engage in activities ranging from consultations on study design through the development and evaluation of models, the performance of simulations, and the presentation of results.

Department:Strategic Consulting Services/Clinical Pharmacology and Pharmacometrics

Internal Grade:14

Direct Reports:No

Status: Exempt

Location:Remote

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 with the support of colleagues
• Participate in regulatory interactions with health authorities
• 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 for noncompartmental analyses, using Gastro Plus, 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 for reports and documents
• 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
• 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
• Provide mentoring and feedback to junior scientists
• Engage in cross-divisional discussions of scientific strategy
• Serve as an expert resource for the Business Development Team
• 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 Gastro Plus, MONOLIX, and other workshops…