Allucent
drug development
AssociateDirector/Director,Pharmacometrician
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“Associate Director/Director, Pharmacometrician at Allucent. Skills: modeling and simulation, population PK analyses, clinical pharmacology, pharmacometrics, regulatory interactions. Lead and conduct population PK analyses using advanced modeling tools and methodologies. Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis”
What You'll Achieve.
deliver high-impact insights; drive results
Industry & Context.
solving complex scientific challenges; sharp analytical thinking
minimum of 2 days in office per week for employees within a reasonable distance from one of our global offices
What They're Looking For.
Must Have
6-10 years of experience in drug development and pharmacometrics, Regulatory experience including regulatory report writing, Experience with regulatory submissions including INDs, CTAs, regulatory meetings and NDALA/MAA submissions, Life science, healthcare and/or business degree, Minimum 6-10 years of relevant work experience, including experience in drug development, clinical pharmacology, and pharmacometrics
Nice to Have
Proficiency in NONMEM, Pirana, and R software
What You'll Do.
Lead and conduct population PK analyses using advanced modeling tools and methodologies
Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis
and interpret clinical pharmacology studies
Provide strategic guidance to clients
owning deliverables and developing clinical pharmacology plans
Author and review PK reports and clinical pharmacology sections of regulatory documents
Represent clients in regulatory interactions and contribute to business development and relationship management
How You'll Work.
Team & Collaboration
guide teams; mentor pharmacometricians; collaboration
Communication Scope
communication; negotiating skills
Full Job Description
**Associate Director/Director, Pharmacometrician** Step into a role where science meets strategy and your expertise shapes the future of drug development. As an Associate Director(AD)/Director, Pharmacometrician, you’ll lead high-impact modeling and simulation efforts within a dynamic Clinical Pharmacology, Modeling and Simulation (CPMS) environment. You’ll guide teams, mentor pharmacometricians, and provide strategic insight to clients at key development milestones. This role also offers the opportunity to represent clients in interactions with regulatory agencies. If you thrive on collaboration and solving complex scientific challenges, this is your chance to make a meaningful impact. _About the role_ This role combines scientific leadership and strategic impact, leading population PK analyses while developing innovative approaches to improve efficiency and accuracy. You will design, analyze, and interpret clinical pharmacology studies, provide strategic guidance to clients, and contribute to regulatory documents and agency interactions. In addition, you’ll foster client relationships, support business development, and stay at the forefront of PK/PD advancements to drive continuous improvement. **Your main responsibilities will include but not limited to:** * Lead and conduct population PK analyses using advanced modeling tools and methodologies * Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis * Design, analyze, and interpret clinical pharmacology studies (renal, hepatic, TQT, ADME, DDI, BE/BA, SAD, MAD, etc.) and provide guidance to optimize pharmacokinetic sampling and dosing strategies * Provide strategic guidance to clients, owning deliverables and developing clinical pharmacology plans * Author and review PK reports and clinical pharmacology sections of regulatory documents * Represent clients in regulatory interactions and contribute to business development and relationship management **Requirements** _About
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