Senior Biostatistician (FSP + Remote)

Cytel; Países Baixos; Teletrabalho; EUR 90 000 - 130 000; Tempo integral

Resumo da oferta

Cytel Netherlands seeks an experienced Senior Biostatistician to lead or support Phase I–IV clinical studies, embedded within a pharmaceutical client. You will perform advanced analyses, develop SAPs, and prepare integrated summaries for submissions, collaborating across clinical and regulatory teams.

You will work with SAS and R, ensure CDISC/ADaM compliance, and maintain robust programming standards while fostering strong cross-functional relationships across global teams.

Qualificações

• Bachelor's degree is required in statistics or related field.
• 5+ years of clinical trials experience in pharma/biotech or CRO.
• Experience with SAS, R, and regulatory submissions.
• Strong communication and cross-functional collaboration skills.

Responsabilidades

• Provide statistical support to clinical studies.
• Participate in study protocol development and design discussions; assist with sample size calculations.
• Review CRFs and data review guidelines; develop SAPs and analysis datasets.
• Perform statistical analyses and interpret results; prepare safety and efficacy summaries.
• Prepare clinical study reports including integrated summaries for submissions and regulatory questions.
• Communicate methodology and implications clearly to stakeholders; ensure compliance with FDA/GxP guidelines.
• Contribute to standards for programming tools, outputs, and macros; collaborate with CROs and vendors.
• Assist in CRFs, edit checks, and data validation plans; may review data transfers.
• Support timely project delivery through cross-functional collaboration.

Conhecimentos

Clinical trials

SAS programming

R programming

CDISC/ADaM

Statistical analysis

Regulatory submissions

Communication skills

Team leadership

Formação académica

Bachelor's degree in statistics or related discipline

Ferramentas

SAS

R

ADaM standards

CDISC standards

Descrição da oferta de emprego

Who Are You?

An experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-IV clinical studies. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same.

Sponsor-dedicated:

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

Our Senior Biostatisticians perform ad-hoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus, for example, if you understand the regulatory questions and translating them to statistical problems, collaborating effectively, with clinical and regulatory colleagues. Supporting medium complexity clinical trials (starting from Design to Archival experience) and supporting some project-level activities.

As a Senior Biostatistician, your responsibilities will include:

• Providing statistical support to clinical studies
• Participating in the development of study protocols, including participation in study design discussions and sample size calculations
• Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications
• Performing statistical analyses and interpreting statistical results
• Preparing clinical study reports, including integrated summaries for submissions
• Utilizing your strong communication skills to present and explain the methodology and consequences of decisions.
• Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
• Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
• Participate in the development of CRFs, edit check specifications, and data validation plans
• Provide review and/or author data transfer specifications for external vendor data
• Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
• Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

• Minimum of Bachelor's degree in statistics or a related discipline.
• 5+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Experience working for a CRO is strongly desired.
• Experience in sample size calculation, protocol concept development, protocol development, SAP, and preparing clinical study reports including integrated summaries for submissions.
• Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. Knowledge of R programming is a plus.
• Solid understanding & implementation of CDISC requirements for regulatory submissions.
• Adept in ADaM specifications generation and QC of datasets.
• The ability to build strong external & internal relationships and motivate a regional or global team.
• Effective communicator: able to explain methodology and consequences of decisions in lay terms.

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Cytel Inc. is an Equal Employment / Affirmitive Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.