Principal Statistician - Permanent Role -Remote in UK

ClinchoiceRemotesenior

In short

▸Liderar análisis estadísticos en ensayos clínicos desde la estrategia hasta los informes.
▸Trabajar remotamente en Reino Unido con equipos multidisciplinarios y clientes globales.
▸Destacar como autor principal de documentos clave como SAPs y secciones estadísticas en informes.

Fluent written and spoken English required.

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What they ask for

✓Título de estadística, matemáticas, biometría o campo afín.
✓Experiencia sólida en estudios clínicos en farmacéutica o biotecnología.
✓Capacidad para liderar proyectos estadísticos de forma independiente.
✓Habilidades avanzadas en programación estadística (SAS, R o Python).
✓Conocimiento profundo de guías regulatorias (ICH, FDA, EMA).
✓Excelentes habilidades de comunicación escrita y oral en inglés.

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SASRPythonClinical DatabaseStatistical Analysis Plans (SAAnalysis Database SpecificatioClinical Study Reports (CSRs)ICH guidelinesFDA regulationsEMA guidelines

Who should you write to at Clinchoice?

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ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Principal Statistician to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes. We are seeking a highly skilled Principal Statistician to lead statistical activities for clinical trials. This role requires hands-on statistical expertise, strong communication skills, and the ability to independently lead projects while collaborating closely with cross-functional teams. Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career! Key Responsibilities • Lead and provide statistical support for clinical studies. • Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables • Author and review key statistical documents, including: • Statistical Analysis Plans (SAPs) • Analysis Database Specifications (ADS) • Statistical sections of clinical study reports • Review and interpret analysis outputs, ensuring accuracy, quality, and regulatory

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