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Posted May 13, 2026

Non-Clinical CMC Statistician, FSP

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About the position Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market. The non-clinical Statistician will employ statistical design, tools, and techniques to support process, analytical method and formulation development of medical or pharmaceutical products throughout their lifecycle. Responsibilities • Collaborate with subject matter experts to design experimental studies, plan and perform statistical analysis, and document results in technical reports, in support of business decisions, regulatory submissions and compliance. • Provide statistical support for a wide range of non-clinical applications, including: particle size and distribution, in-vitro bioequivalence assessments, analytical method optimization and validation, process development and platform characterization, and stability studies to understand, control, and ensure product quality. • Ensure compliance with regulatory and ISO requirements for the statistical methods employed. • Develop, implement, and maintain statistical tools used to support product life cycle activities. • Promote good statistical practice across the team and mentor colleagues in statistical techniques and software tools. • Stay up to date on best practices, industry trends, and regulatory guidance. • Support other non-clinical statistical applications, when needed. • Support regulatory audits by responding to questions during on-site inspections and providing written responses to clarify statistical approaches or perform additional analyses. Requirements • Doctorate Degree in Statistics or a related field plus 2 years minimum of relevant applied statistics experience OR Master’s Degree in Statistics or a related field plus 5 years minimum of relevant applied statistics experience OR Bachelor’s Degree in Statistics or a related field plus 10 years minimum of relevant applied statistics experience. • Proficient in the following: non-clinical applications, including particle size and distribution, in-vitro bioequivalence assessments, analytical method optimization and validation, process development and platform characterization, and stability studies to understand, control, and ensure product quality. • Experience and/or training in design of experiments, including optimization or robustness experimental designs. • Proficient in statistical techniques commonly used in pharmaceutical manufacturing operations, such Statistical Process Control, Process Capability Analysis, Measurement System Analysis, Acceptance Sampling, Non-linear and Linear Regression, Significance Testing, and Simulation. • Proficient in SAS and/or R programming including data manipulation, macros, functions, statistical and graphical packages, and quality output production. • Good understanding of pharmaceutical development and CMC activities in a regulatory context, including GMP and Quality by Design framework. • Excellent communication and collaboration skills. • Demonstrated ability to work independently and pro-actively to deliver top quality work product. Nice-to-haves • Skills in machine learning or Bayesian methods are a plus. • JMP or R-Shiny skills are a plus. Benefits • Home-based remote working opportunities. • Work/life balance as well as flexible schedules. • Collaborating with motivated, high-performance, statistical and research teams. • Technical training and tailored development curriculum. • Research opportunities that match your unique skillset. • Promising career trajectory. • Job stability: long-term engagements and re-deployment opportunities. • Focus on bringing new therapies to market rather than project budgets and change orders. • Experience with regulatory submissions. • Engaging, fast-paced environment. • Good work-life balance. Apply tot his job Apply To this Job