new opportunties

Dear All, I wanted to reach out to you today to discuss a few new open positions with some of our top clients. Below is a brief description of each role. If interested please schedule a time to speak with our Recruiter, Elizabeth Busch at https://meet.yesware.com/me/elizabeth13/30min. *Principal Scientist Clinical Pharmacology* *Key Responsibilities* Support the clinical development and translational sciences programs. Build pharmacostatistical models for population PK/PD and exposure-response analyses. Conduct meta-analysis and provide scientific input for dosage selection and study designs. Contributes to clinical pharmacology strategy and prepares modeling reports for regulatory submissions. *Job Requirements* Ph.D. in Clinical Pharmacology, Pharmaceutical Sciences, or related field. 3+ years of industry experience. Experience using modeling software such as NONMEM, R, Python, etc. Experience analyzing data using modeling and simulation expertise. *Principal/Senior Scientist Clinical Pharmacology* *Key Responsibilities* Lead the development of quantitative clinical pharmacology and modeling strategies for cutting-edge therapies. Apply advanced modeling approaches, such as PK/PD, PBPK, and quantitative systems pharmacology to ensure safe and effective dosing. Utilize model-based drug development principles for optimal drug development. *Job Requirements* Ph.D. in Pharmacokinetics, Pharmaceutical Sciences, or related field. 5+ years' experience in clinical pharmacology and modeling & simulation needed. Must excel in quantitative clinical pharmacology and have a strong track record in model-based drug development. Responsibilities include leading clinical studies and engaging with global health authorities. *Senior Principal Scientist/Associate Director Clinical Pharmacology, Modeling & Simulation* *Key Responsibilities* Responsible for conducting and overseeing clinical pharmacology studies and analyses to support project decisions and regulatory requirements. Lead the design and execution of phase I clinical studies and provide dosing recommendations to project teams. Contribute to regulatory documents and address queries from regulatory agencies. *Job Requirements* Ph.D. in Clinical Pharmacology, Pharmaceutical Sciences, or related field. 7-10+ years of industry experience. Experience in clinical pharmacology management and quantitative drug development, including PK modeling. Proficient in designing and reporting studies for regulatory submissions.