Principal Statistician

JR United Kingdom; Newcastle upon Tyne; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization is seeking a Principal Statistician to join its study delivery team in Newcastle. The role involves managing biostatistics activities for complex studies while providing mentorship to team members. Candidates should possess an advanced degree in statistics and relevant experience in the field, particularly in respiratory studies. This position offers a competitive salary, flexible working conditions, and an emphasis on professional development.

Benefits

Flexible working platforms

Excellent employment package

Focus on work-life balance

Qualifications

• Experience in statistics or biostatistics highly desirable.
• Experience in respiratory field preferred.
• Knowledge of clinical trials methodology and regulatory requirements essential.

Responsibilities

• Lead Biostatistics and Programming activities on studies.
• Prepare statistical analysis plans and reports.
• Review and ensure quality of study databases and interim reports.

Skills

Leadership

Statistical Analysis

Coaching

Regulatory Knowledge

Protocol Development

Education

M.S. or Ph.D. degree in statistics, biostatistics, or related field

Tools

SAS

Job description

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Principal Statistician, newcastle-upon-tyne, tyne and wear

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Client:

Warman O'Brien

Location:

newcastle-upon-tyne, tyne and wear, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

8

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

We have recently partnered with an award winning CRO, who are looking for an experienced Principal Statistician, to join their successful study delivery team, any area of specialism considered

How you will be a success

The Principal Biostatistician will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of high value with high impact for the organization. Also responsible for planning, monitoring, organizing and reviewing activities of biostatisticians and programmers working on the assigned program of studies, ensuring individual studies and the overall program of studies and integrated analyses are delivered on time, on budget to required quality. Accountabilities also include maintenance of consistency across studies. Regulatory interaction experience also preferred.

• Biostatistical input into the design of the program, Protocol input such as study design, sample size calculations and patient randomization schemes and Statistical aspects of case report form design
• Review project database structures, edit checks and data management coding conventions
• Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
• Statistical analysis, Interpretation of data and reporting of results
• Writing of the statistical methods sections of integrated study reports.
• Reviews draft integrated study reports.
• Supports responses to regulatory questions on the design of the program, and any labelling claims following submission
• Participates in presentations at client and investigator meetings
• Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client.

Key Qualifications and Skills

• M.S. or Ph.D. degree in statistics, biostatistics, or related field.
• Experience in statistics, biostatistics or related field
• Respiratory experience highly desired
• Accountable for leading Biostatistics and Programming activities for a program of studies of high complexity and/or of high value with high impact.
• Ongoing coaching and mentorship of team members.
• Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS are a must.

What you get in return

Ongoing development is vital, and as a Principal Biostatistician you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. In comparison with their competitor’s and pharmaceutical companies, they provide more flexible working platforms for coaching and educating newcomers to be highly respected professionals in our industry.

They also provide successful candidates with an excellent employment package and benefits adapted to the current job market. The company like to look at themselves more like an extended family with consideration of staff as individuals allowing a work-life balance.

What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Statistician onboard as soon as possible.

Not what you are looking for? Please contact Aimee Weston on [phone] for a confidential discussion about potential opportunities.