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Parexel Logo Parexel · Research and Development

Senior Manager, Biostatistician Consultant

United Kingdom · Job Posted January 24, 2026
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Job Description

As a member of Parexel’s Biostatistics group, your expertise in statistical methodology, and data analysis plays a crucial role in providing evidence to support the safety and efficacy of new health treatments. You contribute to research design and analytical strategies, provide input into protocols, and develop and review statistical analysis plans, all while working with the patient in mind.

Job Responsibility

  • Provide broad statistical support, including trial design, protocol and CRF development on specific studies
  • Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
  • Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols
  • Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans
  • Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review
  • Support of Business Development, by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings
  • Understand regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis
  • Understand, apply and provide training in extremely advanced and sometimes novel statistical methods
  • Contribute to the development and delivery of internal and external statistical training seminars and courses
  • Review position papers based on current good statistical practice
  • Interact with clients and regulatory authorities
  • Review publications and clinical study reports
  • Travel to, attend, and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting and discussing study results)

Requirements

  • PhD in Statistics or related discipline, MS in Statistics or related discipline
  • Good analytical skills
  • Good project management skills
  • Professional attitude
  • Attention to detail
  • Thorough understanding of statistical issues in clinical trials
  • Ability to clearly describe advanced statistical techniques and interpret results
  • Familiarity with regulatory/research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines)
  • Prior experience with SAS programming required
  • Ability to work independently
  • Good mentoring/leadership skills
  • Good business awareness/ business development
  • The knowledge of pharmacokinetic data is an advantage
  • Competent in written and oral English

What we offer

  • Flexible work arrangements
  • Opportunities for career growth
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
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