2027 Hiring Opportunities – Senior/Principal Statistician Consultant (Remote in EU)
Core
Provide statistical leadership and expertise across clinical development programs in the pharmaceutical industry, supporting evidence generation and regulatory submissions.
Role type
Senior/Principal Statistician Consultant
Builds
Clinical study reports, regulatory submissions, and integrated summaries of safety and efficacy
Domain
Pharmaceutical/Biotechnology clinical development
Required skills
Clinical trial design, statistical inference, sample size determination, power calculations, regulatory compliance, SAS, R, oncology, rare diseases, neuroscience
Preferred skills
Mentorship, complex trial designs, advanced statistical methodologies
Responsibilities
Lead clinical trial design including endpoint selection and randomization strategies; Develop and review statistical analysis plans (SAPs) and clinical study protocols; Oversee statistical analyses and interpretation of clinical trial data; Provide statistical expertise for regulatory submissions and interactions with health authorities; Collaborate with cross-functional teams including Clinical Development and Regulatory Affairs; Review statistical outputs (TLFs) for accuracy; Contribute to clinical study reports (CSRs) and integrated summaries; Identify statistical risks and recommend solutions; Provide technical guidance and mentorship to team members.