Principal Statistician

JR United Kingdom; Kingston upon Hull; On-site; GBP 50,000 - 80,000; Full time

Job summary

A leading company in the clinical research sector is seeking a Principal Statistician to join their esteemed team. The successful candidate will oversee biostatistics and programming for critical studies, with a focus on ensuring high-quality outcomes. This role offers significant career progression opportunities, a solid mentorship program, and promotes a healthy work-life balance. With competitive salary packages and an inclusive work environment, this position is tailored for those aiming to excel in their field.

Benefits

Ongoing career development

Flexible working conditions

Excellent employment package and benefits

Qualifications

• Experience in statistics, biostatistics, or related field required.
• Knowledge of clinical trials methodology needed.
• Respiratory experience highly desired.

Responsibilities

• Accountable for leadership of Biostatistics and Programming activities.
• Preparation of statistical analysis plans and reporting results.
• Review and comment on protocol design and project structures.

Skills

Statistics

Biostatistics

Data Interpretation

Regulatory Interaction

Statistical Software

Education

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

Tools

SAS

Job description

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Principal Statistician, kingston upon hull, east yorkshire

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Client:

Warman O'Brien

Location:

kingston upon hull, east yorkshire, 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.