Associate Director, Pharmacometrics (Pop PK and PK/PD)

Simulations Plus• US,

2d•$140,000 - $170,000•Remote

About The Position

Simulations Plus is a global leader in model-informed and AI-accelerated drug development, providing innovative science-based software and consulting solutions to clients. The Associate Director, Pharmacometrics will lead cross-functional project teams to achieve client goals, engaging in activities such as study design consultation, model development and evaluation, simulations, and results presentation. This role is within the Strategic Consulting Services/Clinical Pharmacology and Pharmacometrics department and is a fully remote position with flexible scheduling.

Requirements

Proficiency in Monolix, NONMEM, and R
Proficient at developing and delivering presentations
Highly self-motivated and willing to take on challenges
Possess excellent critical-thinking, problem-solving, and interpersonal skills
Strong verbal and written communication

Nice To Haves

6+ years of population PK and PK/PD professional modeling experience preferred
Professional experience in application of Pharmacometrics to Clinical Pharmacology preferred

Responsibilities

Independently develop and evaluate complex models and simulations
Lead, manage, and collaborate effectively with cross-functional project teams to successfully support client requests
Build partnerships with clients; provide strategic input and advice
Serve as main point of contact for assigned clients and projects
Consult with clients on study design through development and evaluation of models
Provide valuable insight into the optimal use of modeling and simulation in drug development programs
Clearly communicate and present modeling and simulation results to clients
Use state-of-the-art software to develop, evaluate and apply PK, PK/PD and exposure-response models
Formulate pharmacometric data analysis plans and data requirement documents, ensuring appropriateness of methods for data handling and analysis and compliance with current global regulatory guidance
Perform model-based simulations to address critical development questions
Write pharmacometric reports and regulatory documents
Utilize internal resources to meet project timelines and budgets
Share scientific knowledge and skills with other staff members
Other duties as assigned