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# Statistical Scientist Director

- **Company:** Premier Research
- **Location:** UK
- **Contract:** Permanent contract
- **Skills:** Computer Programming, SAS (Software)
- **Published:** September 21, 2026
- **Apply:** https://www.apply4u.co.uk/jobs/statistical-scientist-director/47784804

## About the Role

expectations (FDA, EMA, PMDA, etc.).Support business development through participation in bid defenses, capabilities presentations, RFP strategy and build trusted scientific relationships with sponsors and influence decision-making through evidence-based recommendations.Acts as an independent biostatistician on DSMBs and DMCsWhat We Are Searching ForAdvanced degree (MS or PhD) from accredited college or university, in statistics or closely related field. Equivalent combination of education, training and experience will be considered.15+ years' experience in clinical trials design and analysis, preferably in a CRO environmentAt least 1 yr technical experience in clinical trials design and analysis implementing innovative statistical analysis.Previous experience implementing innovative statistical designsStrong knowledge of regulatory, scientific, technical and clinical expertise in conduct of clinical trials in the respective area of focus as demonstrated by past positions related to the
therapeutic area in the CRO and Pharma/Biotech sectorStrong computer skills, with knowledge of advanced programming skills with standard software, including SAS, RExcellent working knowledge of CDISC standards and application of these standards to projects.Ability to manage and de-escalate difficult situations with clients, teams, and managementDemonstrated experience in interacting with regulatory agencies (e.g., FDA, EMA, EU member states)Excellent English and Host Country Communication skills (verbal, written & interpersonal).Excellent organizational and time-management skills, able to prioritize work to handle multiple tasks and meet deadlines in a dynamic environmentA willingness to travel, ~20%SummaryLocation: United KingdomType: Full time

## Description

planning through reporting, ensuring alignment of design, analyses, and data interpretation.Communicate complex quantitative concepts clearly to non-statistical stakeholders-including sponsor leadership, regulatory representatives, and clinical teams.Develops sample size estimation, modeling approaches, adaptive or Bayesian frameworks, and innovative trial designs.Develops or provides senior oversight for statistical deliverables, including: statistical selection of protocols, statistical Analysis Plans (SAPs), randomization specifications and Statistical contributions to CSRs, publications, and regulatory documentsIdentify risks related to study design, sample size, or analysis approaches and proactively propose mitigation strategies.Acts as project manager for biostatistics stand-alone work and drive high-quality statistical deliverables while managing budget, scope, and timeline expectations.Advise clients on regulatory guidelines, statistical principles for submissions, and global


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