ClinChoice - 2027 Hiring Opportunities – Senior/Principal Statistician Consultant (Remote in UK- Outside IR35)

United Kingdom2w ago

In Office Principal EMEA Medical Devices Pharmaceuticals Statistician Principal Reporting CRO Clinical Trials Documentation Close

Requirements

• oncology, rare diseases, and/or neuroscience. • The Application Process • Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. • Who will you be working for? • ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. • Our Company Ethos • Our Company Ethos • Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

Responsibilities

• Provide statistical leadership across clinical development programs, from early-phase studies through late-phase clinical trials. • Lead clinical trial design, including endpoint selection, sample size calculations, power analyses, and randomization strategies. • Develop and review clinical study protocols, statistical analysis plans (SAPs), and other statistical documentation. • Oversee statistical analyses and interpretation of clinical trial data to ensure scientific rigor and regulatory compliance. • Provide statistical expertise for regulatory submissions and interactions with health authorities, including the FDA and EMA. • Collaborate with Clinical Development, Clinical Operations, Data Management, Regulatory Affairs, and Medical Writing teams. • Review statistical outputs, including tables, listings, and figures (TLFs), to ensure accuracy and consistency with analysis plans. • Contribute to clinical study reports (CSRs), integrated summaries of safety and efficacy, and other regulatory documents. • Identify statistical risks and recommend appropriate solutions throughout the clinical development process. • Provide technical guidance and mentorship to statisticians and other team members, as appropriate.