Associate Director, Pharmacometrics

Overview Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries. At Certara, we accelerate medicines to patients by partnering with life science innovators. In the past 6 years, over 90% of companies that received new drug approvals by the FDA used our software or services. Our integrated and proprietary end-to-end platform with biosimulation, regulatory science, and market access solutions combined with our strong team of scientists and subject matter experts enable our clients to have: Informed decision-making & reduced clinical trial burden Higher R&D productivity Improved patient outcomes & increased patient access to medicines Accelerated regulatory approval Certara is a global team that fosters and nurtures a diverse and inclusive culture. We are proud to be an Equal Opportunity Employer. The collective sum of our individual differences, life experiences, knowledge, innovation, self-expression, and unique capabilities and talent represents a significant part of our culture, our reputation and our achievement. Together with our partners, we use biosimulation and technology-enabled services to transform drug discovery and development across all therapeutic areas and innovative therapies. Our Pharmacometricians are responsible for supporting quantitative decision-making in drug development through the development and application of population PK, PK/PD, exposure-response and other models. Qualified candidates will have the ability to work on a variety of therapeutic indications and data types and must be experts in applied Population PK, PK/PD, and/or exposure-response modelling and simulation to support drug development. We are looking for Pharmacometricians that want to: Deepen their strategic drug development expertise and their experience informing drug development decisions. Hone their pharmacometric techniques with fit-for-purpose modelling approaches leveraging e.g. model-based meta‑analysis, target‑mediated drug disposition models, and E‑R trial simulations. Broaden their drug development expertise by working with a myriad of companies, molecular modalities, and therapeutic areas. Develop their consulting career path by recognizing and seeking opportunities that match their ambition and personal interests. Responsibilities Support projects for Certara’s clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e.g. IT, methodology, efficiency, automation, quality). May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications PhD, MD, PharmD in Bioengineering, Pharmaceutical Sciences, Pharmacology, Statistics, Applied Mathematics, Engineering, Medicine, or related field. 1 to 5 years of industry/consulting experience (may be combined with academic research) working in R&D, pre‑clinical and clinical environments. Solid experience in pharmacometrics, clinical pharmacology, pharmacokinetics, or a related discipline in a project team setting is preferred, whether in academia or industry. Expertise in PK/PD modelling with strong quantitative skills applied to develop models with nonlinear behavior, mechanistic or semi‑mechanistic components relating to mechanism of action and tailored to meet specific drug‑development questions. Proficiency in PK/PD and statistical software (e.g., NONMEM, R). Proficient in modeling (e.g., popPK and PK/PD analyses, model‑based meta‑analysis, dose‑response and exposure‑response analyses, dataset creation, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling). Experience in moving compounds through the clinical trials process and experience with various elements of clinical development and trial design and management and filings preferred. Independent performance of analysis and modeling and development of reports with limited supervision. Comfortable in a client environment able to communicate with and collaborate with peer scientists. Developing ability to identify new business development opportunities through client interactions. Proficient in spoken and written English. Certara is a global company, and additional languages are of benefit. Travel