Principal Biostatistician – Safety & Trials Strategy

ThermoFisher Scientific; Nederland; Híbrido; EUR 90 000 - 130 000; Tempo integral

Resumo da oferta

Thermo Fisher Scientific is seeking a Principal Scientist in Biostatistics to advance life‑changing therapies through statistical excellence. You’ll lead statistical tasks across study design, analysis, and reporting within our Global Clinical Research team.

In this FSP role, collaborate with clients and internal experts, applying CDISC standards and ICH-GCP guidelines to ensure high-quality results while managing multiple trials and communicating findings clearly to stakeholders.

Qualificações

• Advanced degree in Statistics/Biostatistics or related field with substantial clinical research experience.
• Bachelor’s degree with 8 years of biostatistical experience acceptable in lieu of an advanced degree.
• Expert-level SAS programming and statistical methodology knowledge.
• Strong understanding of ICH-GCP guidelines and clinical trial regulations.
• Experience in SAP development and protocol writing is preferred.

Responsabilidades

• Lead diverse statistical tasks across the full clinical trial process from design to final analysis.
• Collaborate with clients within the FSP division and senior statisticians.
• Produce robust statistical analyses, interpretation, and reporting.
• Ensure adherence to CDISC standards and regulatory expectations across studies.

Conhecimentos

SAS programming

Statistical methods

ICH-GCP knowledge

CDISC standards

R software

WinBUGS

EAST

Analysis planning

Regulatory interaction

Trial management

Attention to detail

Communication skills

Problem solving

Formação académica

Advanced degree in Statistics/Biostatistics

Bachelor’s degree in Statistics/Biostatistics

Ferramentas

SAS

R

EAST

WinBUGS

Descrição da oferta de emprego

Thermo Fisher Scientific is seeking a Principal Scientist in Biostatistics to advance life‑changing therapies through statistical excellence. You’ll lead statistical tasks across study design, analysis, and reporting within our Global Clinical Research team.

In this FSP role, collaborate with clients and internal experts, applying CDISC standards and ICH-GCP guidelines to ensure high-quality results while managing multiple trials and communicating findings clearly to stakeholders.