Associate Director, Pharmacometrics, Clinical Pharmacology
Our client is seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission – to identify, develop and deliver life-changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
Position Summary:
The individual will be responsible for the design, leadership, and implementation of Modeling & Simulation strategies across our client’s clinical programs. In this role, you will perform or supervise execution of the pharmacometrics strategy in those programs with focus on implementing model-informed drug development (MIDD) approaches. You will set the strategy for addressing pharmacometric issues and directly influences drug development decisions. The successful candidate will have good quantitative pharmacology skills, scientific reasoning, exploratory graphical analysis skills and report writing skills.
Responsibilities:
- Developing and executing modeling and simulation strategies from the early through late-stage clinical development and serve as the SME in cross-functional development program teams
- Delivering strategic and well-timed modeling input at key decision points along the development path
- Set the strategy for addressing pharmacometric issues in regulatory submissions and directly influences drug development decisions
- Lead and drive PMX contributions to integrate relevant technical and scientific knowledge in the planning and execution of robust quantitative development programs with focus on MIDD strategies
- Use state of the art modeling and simulation approaches to interpret PK/PD data and accountable and responsible for ensuring appropriate PK-PD analysis including population PK, PK-PD modeling and simulation, and exposure-response analysis
- Guide empirical modeling/QSP approaches to understand relationship between PK, biomarkers and disease outcomes undefined
Education/Experience Requirements:
- PhD or PharmD in Pharmaceutical sciences, Clinical Pharmacology, Mathematics, Statistics, Engineering (or equivalent) required
- 4+ years experience of relevant industry experience including NLME methods and its application in Dose-exposure-response analysis, population PK/PD modeling, disease progression modeling and clinical trial simulation
- Clinical pharmacology, statistics and therapeutic knowledge in one or more disease areas
- Experience with incorporation of MIDD strategies into drug development across all phases and responding to questions on dose and regimen justification, study design among others
- Hands-on experience with at least NONMEM and R is strongly preferred.
Additional Skills/Experience/Requirements:
- The ideal candidate will embody our client’s core values: Courage, Community Spirit, Patient Focus and Teamwork.
- Well organized with the ability to multitask, prioritize and manage shifting responsibilities in a small, fast-moving and entrepreneurial environment.
- Ability to manage multiple, complex tasks with competing timelines.
- Strong interpersonal, verbal, and written communication skills.
- Driven, intelligent, passionate about making a difference for patients with rare diseases.
- Self-motivated and can independently manage responsibilities.
- Ability to travel (<10%).