Remote/Hybrid - hybrid in Parsippany, NJ Contract end date: 3/19/27 We are seeking an experienced Biostatistician to support clinical development and post-marketing activities within a pharmaceutical environment. This individual will collaborate with biostatistics, statistical programming, clinical teams, CROs, and external vendors to support the design, analysis, and reporting of clinical studies. Responsibilities Support biostatistical activities across clinical development and post-marketing programs Contribute to the design, analysis, and reporting of randomized controlled clinical trials Develop and review statistical deliverables and analyses Partner with statistical programmers, clinical teams, CROs, and vendors Support CDISC-compliant data standards, including SDTM and ADaM Apply statistical methodologies to support clinical and regulatory decision-making Communicate statistical concepts and results to technical and non-technical stakeholders Manage multiple projects and timelines while maintaining high-quality deliverables Qualifications Master's degree in Statistics, Biostatistics, or related field 4+ years of biostatistics experience within the biotechnology or pharmaceutical industry Experience with randomized controlled clinical trials Strong knowledge of clinical trial design, including adaptive designs Extensive hands-on experience with CDISC, SDTM, and ADaM Strong SAS programming experience Knowledge of pharmaceutical regulatory requirements and guidelines Strong communication and cross-functional collaboration skills Preferred Experience with R Regulatory submission/interaction experience Knowledge of real-world evidence, observational research, or causal inference Experience supporting acute or chronic pain clinical programs #J-18808-Ljbffr BioPhase
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