Associate/Director, Clinical Pharmacology Modeling & Simulation - Any Region - Home Based
Our Client currently have TWO tremendous opportunities available to join this extremely collaborative and super friendly team! If you're looking for an opportunity to expand professionally, do more than a narrow scope of work, work alongside a large team of CPMS experts, and provide solutions to a variety of clients with various products in different stages of development across multiple therapeutic areas, we would love to connect! · Serve as a primary source of scientific support for the design, analysis, reporting, and presentation of PK data from clinical trials covering all phases of drug development · Analyze clinical PK data as a member of multidisciplinary development teams. · Work with clinical teams to design PK/PD components in various study designs such as first-in-human, Proof of Concept, Phase 2B, bioequivalence and drug-drug interaction studies. · Responsible for the strategic and operational delivery of client programs and projects to timelines, quality expectations and regulatory requirements. · Act as a mentor to less experienced departmental members |
Qualifications: · Depth of experience and relevant experience will determine level of role, Associate Director level role or Director level · Excellent written and verbal English communication skills are required. Chinese language skills are a plus · Advanced science degree (PhD, PharmD, MSc) and/or relevant experience · Significant experience in clinical drug development of both NCEs and biologicals · Demonstrated understanding of the drug development process and a broad knowledge of FDA and EMEA guidelines, as well as global regulatory expectations · Experience using Phoenix WinNonlin to conduct non-compartmental and compartmental analysis · Experience using other software such as NONMEM, GastroPlus or R are desirable · Strong non-compartmental analysis experience · Previous popPK and/or PBPK experience are a plus · Excellent interpersonal, verbal and written communication skills · Extensive clinical/scientific writing skills · Client focused approach to work ethic · Exhibits and promotes a flexible attitude with respect to work assignments and new learning · Ability to direct and manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail · Willingness to work in a matrix environment and to value and promote the importance of teamwork. · Demonstrated understanding of the drug development process and a broad knowledge of FDA and EMEA guidelines, as well as global regulatory expectations Knowledge And Experience · Significant experience with application of clinical pharmacology, modeling and simulation in drug development and clinical trial conduct in pharmaceutical industry, CRO or academia desired · Acknowledged as an expert in the industry · Demonstrated knowledge of regulatory environment as it relates to CPMS and Drug Development Qualified candidates who are seeking full-time or part-time employment will be considered in any of the 41 countries where Our Client has operations.. |
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