Senior Biostatistician — Lead Clinical Trial Analytics

Parexel; England; On-site; GBP 75,000 - 95,000; Full time

Job summary

Parexel is seeking an experienced Biostatistician to lead study design, analysis strategies, and protocol input. You will author and supervise statistical deliverables, mentor staff, and ensure quality control across projects.

This role integrates with global teams to advance clinical research and patient outcomes. Requirements include a Master’s in Statistics or PhD in Statistics (or equivalent) with 4–5 years of industry experience; strong knowledge of clinical trials statistics; and SAS or R

Qualifications

• Master's Degree in Statistics (or equivalent) plus 5 years industry experience OR Ph.D. in Statistics (or equivalent) plus 4 years industry experience
• A thorough understanding of the statistical aspects of clinical trials
• Experience in statistical analysis in a clinically related subject within clinical trials
• SAS programming or R programming skills (desired)

Responsibilities

• Lead research design and analytical strategies for studies.
• Advise, develop and oversee quality control of statistical deliverables.
• Direct Biostatistical activities on a study and ensure timely results.
• Coordinate Biostatistics related project activities within timelines and budget.
• Represent Parexel at client meetings and liaise with teams globally.
• Coach and mentor junior members of the department.
• Collaborate with other departments to optimize efficiency across the study lifecycle.

Skills

SAS programming

R programming

Leadership

Mentoring

English communication

Education

Masters Degree in Statistics

PhD in Statistics

Biostatistics/Statistics/Mathematics degree

Tools

SAS

R

Job description

Parexel is seeking an experienced Biostatistician to lead study design, analysis strategies, and protocol input. You will author and supervise statistical deliverables, mentor staff, and ensure quality control across projects.

This role integrates with global teams to advance clinical research and patient outcomes. Requirements include a Master’s in Statistics or PhD in Statistics (or equivalent) with 4–5 years of industry experience; strong knowledge of clinical trials statistics; and SAS or R