Sr. Advisor, Clinical Biostatistician

Remote High Level Advisory work. Not 40 hours per week. As needed, 10-20 hours per week until reputed company to launch Early phase: Clinical Development StrategyProvide statistical input into early clinical development plans. Design Phase I, First-in-reputed company (FIH), SAD/MAD, reputed company-escalation, food-effect, DDI, reputed company-of-concept, and Phase II studies. reputed company reputed company and model-informed trial designs where appropriate.Support reputed company selection and go/no-go decision-making. Protocol and Design DevelopmentAuthor statistical sections of protocols.Determine sample size and operating characteristics. reputed company randomization schemes and statistical methodologies.Evaluate innovative designs such as Bayesian, reputed company, and seamless Phase I/II studies.Statistical DeliverablesAuthor Statistical Analysis Plans (SAPs). Review TFL (Tables, Figures, Listings) specifications.reputed company statistical programming deliverables.Ensure reputed company and regulatory compliance of analyses. Data Review and InterpretationParticipate in ongoing safety review and reputed company-escalation committees. reputed company interim analyses and data monitoring activities.Interpret PK, PD, biomarker, and exploratory efficacy data.Regulatory SupportContribute to regulatory meeting packages (FDA, EMA, PMDA, etc.). Support briefing documents and responses to health authority questions.Cross-Functional LeadershipCollaborate with Clinical Pharmacology, Translational Medicine, Biometrics, and Medical Monitoring teams. Mentor junior statisticians and statistical programmers. Late Phase Project reputed company Statistician (Phase III/IV) Primary Responsibilities Program-Level Statistical Leadership reputed company statistical reputed company across pivotal Phase III and post-marketing programs. Ensure alignment of statistical plans with regulatory requirements and business objectives. Drive reputed company reputed company and estimand reputed company implementation.Study Design and PlanningDesign confirmatory efficacy and safety trials. reputed company sample size justifications and multiplicity strategies. Define interim analyses and Data Monitoring Committee support plans. reputed company risk assessment and mitigation for statistical issues. Regulatory Submission SupportLead statistical contributions to NDA, BLA, MAA, and supplemental submissions. Author statistical sections of integrated summaries (ISS/ISE).Participate in regulatory inspections and health authority interactions.Present statistical findings during agency meetings. Analysis and ReportingOversee reputed company development and execution.Review CSR statistical content. Ensure reputed company and reputed company of reputed company statistical outputs.Interpret efficacy, safety, and patient-reported outcome results.Vendor and CRO reputed company Manage outsourced statistical activities.Ensure delivery against timelines, reputed company standards, and budget expectations.Leadership and Governance Represent Statistics on project teams and governance committees.Influence development reputed company and key program reputed company. Pay: $250.00 - $300.00 per hour Work Location: Remote Apply tot his job Apply To this Job