Associate Director
vor 4 Wochen
Associate Director / Director – Modeling & Simulation – VAF 317Basel, Europe--Product Development-Biopharmaceutical Drug Development services-Permanent contractAbout usIntiQuan is Product Life Group’s global Center of Excellence in Pharmacometrics, Quantitative Systems Pharmacology, and Clinical Pharmacology, dedicated to delivering cutting-edge solutions to the healthcare and pharmaceutical industries. As we continue to grow, we are seeking an experienced Modeler and Leader to lead and contribute to the execution of client projects.Role OverviewAs a seasoned modeler, you will take a leading role in the execution of client projects, ensuring scientific excellence and strategic alignment. You will actively engage with clients to define project scope, communicate insights, and deliver impactful results. In addition to hands-on modeling and project leadership, you will mentor and support junior team members, fostering their growth and contributing to a collaborative, high-performing team environment.Your ImpactAs Associate Director / Director, you will:Lead and execute advanced pharmacometric analyses (e.g., population PK, PK/PD, exposure-response) across all phases of drug development, including regulatory submissionsServe as scientific lead on client projects, ensuring timely, high-quality deliverables while mentoring junior modelers.Act as a strategic partner to clients – guiding complex discussions, navigating challenges, and shaping development strategies.Provide internal scientific feedback and guidance to project teamsContribute to IntiQuan’s growth by supporting offering development, business development, and go-to-market initiatives.Support building the talent base at IntiQuan by selecting the right candidates, onboarding them, and supporting the professional development of junior colleagues.Represent IntiQuan at external meetings, e.g. scientific conferences.What You Bring10+ years of hands-on experience in pharmacometric modeling in pharma or consulting; Quantitative Systems Pharmacology exposure is a plus.Experience with modeling and reporting for regulatory submission.Deep understanding of drug development processes and regulatory expectations for modeling.Proven leadership in cross-functional teams and client-facing roles.Proficiency in R and either NONMEM or MONOLIX.Experience mentoring and managing junior scientists.Advanced degree (MS or PhD) in a quantitative field (e.g., Pharmacometrics, Bioinformatics, Engineering, Physics).Excellent communication skills in English both oral and written; German or other languages are a plus.A collaborative mindset with the ability to work independently.Location: Basel, Switzerland or Remote (Europe) #J-18808-Ljbffr
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