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Principal Biostatistician Consultant - Remote (experience working with medical affairs and commercial) at ClinChoice. Location Information: . Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….. . ClinChoice is searching for an . Principal Biostatistician Consultant . to join one of our clients.. . ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  . . Position Description:. . We are seeking an experienced Contract Biostatistician to support Medical Affairs and Real‑World Evidence (RWE) activities. The role will provide statistical leadership in the design, analysis, and interpretation of RWE/observational studies, external comparator analyses, and evidence generation strategies to support post‑marketing, payer, and hypothesis generation analysis. This position requires close collaboration with cross-functional teams including Medical, HEOR, Clinical Development, and Commercial.. . Responsibilities and Duties:. . . Partner with medical for publication strategies, HEOR or economic modeling inputs. . Provide statistical expertise in analyses using external control and/or synthetic control, meta-analyses, and causal inference analyses, e.g. propensity score matching method. . Contribute to manuscripts, abstracts and presentations. . Collaborate with HEOR to align analyses with HTA agency expectations. . Review protocols for real world evidence studies. . Work with statistical programmers to conduct ad hoc analyses; Conduct quality review of statistical analyses. . Perform statistical programming for advanced statistical methodologies and help statistical programmers QC their programs. . Review relevant medical literature. . Write statistical analysis plans. . Develop TLF shells and review programming specs.  . . . Minimum Requirements:. . Experience. : . . . M.S., Biostatistics or Ph.D. in Biostatistics or equivalent with at least 5 years of pharmaceutical, biotechnology, or equivalent experience.. . . Other:. . . Prior experience working with medical affairs and commercial. . Good understanding of meta-analyses and causal inference methodologies. . Familiarity with regulatory guidance on RWE and HTA requirements. . Strong statistical reasoning and problem-solving. . Ability to communicate complex methods to non-statistical stakeholders. . High attention to data quality and methodological rigor. . Ability to work independently in a fast-paced, cross-functional environment. . Understand good clinical practice guidelines. . Good statistical programming skills using relevant statistical software. . Oncology experience preferred. . . #LI-TT1 #LI-Remote #Principal#Contract