Allucent
Biotechnology
AssociateDirector/Director,Pharmacometrician
Neural analysis suggests this role is
optimal for Director candidates.
“Associate Director/Director, Pharmacometrician at Allucent. Skills: Pharmacometrics, Population PK, Clinical Pharmacology. Lead population PK analyses. Conduct population PK analyses”
Industry & Context.
Complex scientific challenges
What They're Looking For.
Must Have
6-10 years of experience in drug development, 6-10 years of experience in pharmacometrics, Regulatory experience, Regulatory report writing, Experience with regulatory submissions, Experience with regulatory meetings, Life science degree, Healthcare degree, Business degree
Nice to Have
Proficiency in NONMEM, Proficiency in Pirana, Proficiency in R software, Experience with INDs, Experience with CTAs, Experience with NDALA submissions, Experience with MAA submissions
What You'll Do.
Lead population PK analyses
Conduct population PK analyses
Develop innovative approaches
Implement innovative approaches
Enhance efficiency of PK analysis
Enhance accuracy of PK analysis
Design clinical pharmacology studies
Analyze clinical pharmacology studies
Interpret clinical pharmacology studies
Provide guidance to optimize sampling
Provide guidance to optimize dosing
Provide strategic guidance to clients
Own client deliverables
Develop clinical pharmacology plans
Author regulatory documents
Review regulatory documents
Represent clients in regulatory interactions
Contribute to business development
Contribute to relationship management
How You'll Work.
Team & Collaboration
Client interactions; Regulatory agencies
Communication Scope
Regulatory report writing; Client communication
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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