Director, Pharmacometrics

The Director, Pharmacometrics role at Allucent places you at the intersection of scientific leadership and strategic impact within a vibrant Clinical Pharmacology, Modeling and Simulation (CPMS) environment. Allucent's mission is to bring new therapies to light by partnering with clients to develop innovative pharmaceuticals and biologics, and this position is central to shaping those drug‑development programs. In day‑to‑day work you will lead and conduct population pharmacokinetic (PK) analyses using advanced modeling tools, devise new methods that boost efficiency and accuracy, and design, analyze and interpret a wide range of clinical pharmacology studies, including renal, hepatic, thorough QT, ADME, drug‑drug interaction, bioequivalence/bioavailability, single‑ascending‑dose and multiple‑ascending‑dose trials. You will own deliverables, craft clinical pharmacology plans, author and review PK sections of regulatory dossiers, and guide clients on optimal sampling and dosing strategies. The role also involves representing clients in regulatory agency interactions and contributing to business‑development and relationship‑management activities. To succeed, you need a life‑science, healthcare or business degree together with at least ten years of relevant experience in drug development, clinical pharmacology and pharmacometrics. A solid background in regulatory work is essential, including writing regulatory reports and handling submissions such as INDs, CTAs, and NDA/BLA/MAA packages. Strong analytical thinking, client focus and natural leadership are expected, as is the ability to thrive in fast‑paced, collaborative settings. Allucent offers a comprehensive benefits package, competitive salaries, a departmental training budget, flexible working hours and the possibility of remote or hybrid work depending on location. The position provides leadership and mentoring opportunities, participation in a buddy program, internal growth pathways, and eligibility for spot‑bonus and loyalty award programs. The company's culture emphasizes entrepreneurship, teamwork and continuous improvement. What the role asks for: - Life science, healthcare or business degree - Minimum 10 years relevant work experience - Experience in drug development, clinical pharmacology and pharmacometrics - Regulatory experience including report writing - Experience with IND, CTA, NDA/BLA/MAA submissions - Proficiency in NONMEM, Pirana and R software (nice-to-have) - Excellent organizational, negotiating and financial skills (nice-to-have)