Embedded Senior Biostatistician - Clinical Trials Lead

Cytel; España; On-site; EUR 90,000 - 120,000; Full time

Job summary

Cytel is seeking an experienced Senior Biostatistician to support or lead Phase I–IV clinical studies with advanced statistical methods. You will collaborate with clients and cross-functional teams to drive regulatory submissions and Health Authority responses.

The role embeds you within a sponsor client, enabling ownership and autonomy while contributing to Cytel’s innovation in clinical development. Strong SAS/R programming and CDISC/ADaM expertise are valued as essential for success.

Qualifications

• Master’s degree in statistics or related field; PhD strongly desired.
• 5+ years supporting clinical trials in pharmaceutical/biotech industry.
• Experience with CROs is strongly desired.
• Experience in sample size calculations, protocol development, SAPs, and clinical study reports.

Responsibilities

• Provide statistical support to clinical studies.
• Participate in study design discussions and sample size calculations.
• Review CRFs and data review guidelines; develop SAPs and TLG specs.
• Perform statistical analyses and interpret results.
• Prepare clinical study reports, including integrated summaries for submissions.
• Explain methodology and decisions clearly to stakeholders.

Skills

Statistical analysis

SAS programming

R programming

Regulatory knowledge

Project coordination

Communication skills

Education

Master's degree in statistics

PhD preferred

Tools

CDISC

ADaM

Job description

Cytel is seeking an experienced Senior Biostatistician to support or lead Phase I–IV clinical studies with advanced statistical methods. You will collaborate with clients and cross-functional teams to drive regulatory submissions and Health Authority responses.

The role embeds you within a sponsor client, enabling ownership and autonomy while contributing to Cytel’s innovation in clinical development. Strong SAS/R programming and CDISC/ADaM expertise are valued as essential for success.