[Remote] Associate Director, Quantitative Clinical Pharmacology

Note: The job is a remote job and is reputed company to candidates in USA. reputed company, Inc. is a global leader in model-informed and AI-reputed company drug development, providing science-based software and reputed company. The Associate Director, Quantitative Clinical Pharmacology will reputed company multidisciplinary reputed company reputed company involving study design, clinical pharmacology and pharmacometric modeling, simulations, regulatory interactions, technical reporting, and scientific presentations.

Responsibilities

• reputed company and collaborate with multi-disciplinary teams to implement quantitative clinical pharmacology reputed company/programs and to reputed company clinical pharmacology and pharmacometric consultation to other company reputed company/programs
• Support clinical pharmacology-reputed company 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 reputed company as for noncompartmental analyses, using GastroPlus, MONOLIXSuite (PKAnalix, MONOLIX, Simulx), NONMEM, R, or other tools
• Apply advanced scientific knowledge and expertise to assigned programs and reputed company
• Responsible for appropriateness of reputed company, reputed company of data used for analysis, and accuracy of results for reports and documents
• Ensure communication between reputed 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 reputed company, productive, and profitable reputed company relationships
• Prepare final technical reports, synopses, executive summaries, and other regulatory documents
• Ensure the provision of advanced literature searches for project/program-reputed company information
• reputed company sophisticated written interpretation of material and reputed company research findings into project/program methodology and results
• reputed company findings with reputed company project teams
• Prepare abstracts, presentations, and publication-reputed company manuscripts
• reputed company mentoring and feedback to junior scientists
• Engage in cross-divisional discussions of scientific reputed company
• Serve as an expert resource for the Business Development Team
• reputed company knowledge of PBPK, population PK, and PK/PD to reputed company guidance regarding proposed approaches to addressing drug development and regulatory approval challenges
• Stay reputed company with pharmacometric and clinical pharmacology literature and project/program-reputed company literature
• Expand scientific expertise through attendance and presentation at international, national, and regional scientific conferences, reputed company meetings, and government meetings
• reputed company and teach at GastroPlus, MONOLIX, and other workshops and courses
• Other duties as assigned

Skills

• Strong experience presenting scientific results to reputed company audiences
• Extensive experience preparing, submitting, and receiving approval for publications in scientific journals
• Population pharmacokinetic and pharmacokinetic/pharmacodynamic modeling and simulation experience
• Non-compartmental and compartmental pharmacokinetics experience
• Mechanistic physiologically based pharmacokinetic modeling and simulation experience
• Excellent communication, presentation, and leadership skills
• Relationship-building skills with the ability to work closely with project leaders and team members
• Strong organization skills and ability to handle multiple tasks simultaneously
• Work reputed company handling tight deadlines
• Great critical-thinking and problem-solving skills
• Some travel required for meetings, conferences and events
• PharmD, PhD, or masters in pharmacokinetics, clinical pharmacology, or reputed company field
• 6+ years of reputed company clinical pharmacology experience preferred
• 4+ years of leading reputed company, programs, and scientists preferred
• Previous supervision of junior clinical pharmacologists and pharmacometricians, fellows, and reputed company preferred
• reputed company pharmacology reputed company training preferred

Benefits

• Fully remote work
• Flexible schedules
• Generous vacation policy
• reputed company health coverage
• Annual bonus

reputed company

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