Remote Senior Principal Biostatistician, Clinical Trials

Jazz Pharmaceuticals; Dublin; Remote; EUR 120,000 - 180,000; Full time

Job summary

Jazz Pharmaceuticals is seeking a Senior Principal Statistician to lead statistical aspects of Phase I–IV clinical studies and regulatory filings. You will design analyses, validate results, and partner with cross‑functional teams to ensure robust statistical strategy and high-quality documentation.

Remote work options are available, with emphasis on collaboration and regulatory readiness. The role requires advanced degrees in statistics with substantial pharma/biotech experience, strong SAS and

Qualifications

• MS or MPH in statistics or related field with >4 years in pharma/biotech.
• PhD in statistics or related field with >2 years in pharma/biotech.
• Knowledge of drug development regulations pertaining to statistics.
• Experience with Bayesian/adaptive design preferred.
• Excellent writing and communication skills; leadership abilities.

Responsibilities

• Lead statistical design and analysis for studies and integrated summaries.
• Prepare and review statistical analysis plans and validation activities.
• Develop statistical strategy and analyses for regulatory filings.
• Collaborate with cross-functional teams and external vendors.
• Respond to regulatory questions and participate in agency meetings.
• Ensure timely, high-quality statistical deliverables across trials.

Skills

Statistical design and analysis

SAS

R programming

Regulatory knowledge

Communication skills

Time management

Team collaboration

Leadership

Education

MS or MPH in statistics or related

PhD in statistics or related (preferred)

Tools

CDISC standards

Job description

Jazz Pharmaceuticals is seeking a Senior Principal Statistician to lead statistical aspects of Phase I–IV clinical studies and regulatory filings. You will design analyses, validate results, and partner with cross‑functional teams to ensure robust statistical strategy and high-quality documentation.

Remote work options are available, with emphasis on collaboration and regulatory readiness. The role requires advanced degrees in statistics with substantial pharma/biotech experience, strong SAS and