Principal Biostatistician

buscojobs España; Toledo; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Principal Biostatistician with substantial experience in CRO or pharmaceutical companies. You will lead statistical projects, contribute to clinical study protocols, and ensure the quality of statistical analyses. The role requires strong communication skills and a PhD in a relevant field. Competitive compensation and a commitment to professional development are offered.

Servicios

Comprehensive reward package

Continuous learning opportunities

Equal opportunity employer

Formación

• PhD in relevant field with 5+ years experience in CRO or pharmaceuticals.
• Strong knowledge of CDISC standards and regulatory requirements.
• Proficient in R programming, ESTIMANDS, adaptive designs, and writing SAPs.

Responsabilidades

• Serve as the responsible biostatistician on clinical trials.
• Develop Statistical Analysis Plans and perform senior quality review.
• Oversee outsourced trials from a Biostatistics perspective.

Conocimientos

Leadership

Communication

R programming

ADaM

TFL programming

Educación

PhD in statistics, biostatistics, or related field

Master’s degree with 10+ years of experience

Descripción del empleo

As a Principal Biostatistician, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing :

• Serve as the responsible biostatistician on clinical trials.
• Contribute to clinical study protocols.
• Develop Statistical Analysis Plans and / or perform senior quality review of statistical analysis plans.
• Review and interpret results from simple to complex clinical studies.
• Provide input in the development and review of CRFs.
• Perform lead review and QC of TFLs.
• Critically review derived datasets specifications and datasets (ADaM).
• Present key results.
• Contribute to clinical study reports.
• Review randomization specifications and schemes.
• Oversee outsourced trials from a Biostatistics perspective.
• Contribute to press releases and scientific publications.

You are :

• PhD in statistics, biostatistics, or related field with 5+ years of experience in CRO or pharmaceutical companies OR a Master’s degree with 10+ years of experience.
• Thorough knowledge of CDISC standards and regulatory requirements.
• Experience with Phase 2 and 3 studies.
• Proficiency in R programming, ESTIMANDS, adaptive designs, and writing SAPs.
• Experience in analysis creation for publications.
• Strong leadership and communication skills.
• Knowledge of ADaM and TFL programming.

Why ICON?

We offer a comprehensive reward package, including competitive pay, variable incentives, and employee benefits. We are committed to continuous learning and professional development. ICON is an equal opportunity employer dedicated to a discrimination-free workplace. If you require accommodations during the application process, please let us know. We encourage all qualified individuals to apply, regardless of whether you meet every requirement.

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