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Principal Statistician

JR United Kingdom

United Kingdom

Remote

GBP 50,000 - 90,000

Full time

6 days ago
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Job summary

An established industry player is seeking a Principal Biostatistician to join their dynamic team. In this rewarding role, you will lead biostatistics and programming activities for impactful studies, ensuring high-quality delivery on time and within budget. You will engage in diverse responsibilities, including statistical analysis, regulatory interactions, and mentoring team members. This organization values ongoing development, offering flexible working platforms and a supportive culture that promotes work-life balance. Join a company that prioritizes accountability, collaboration, and integrity, making a significant difference in patients' lives through innovative drug development.

Benefits

Flexible working hours
Career development opportunities
Excellent employment package
Work-life balance

Qualifications

  • Experience in leading biostatistics and programming activities for complex studies.
  • Knowledge of clinical trials methodology and regulatory requirements.

Responsibilities

  • Lead biostatistics and programming activities ensuring timely delivery of studies.
  • Prepare statistical analysis plans and review project database structures.

Skills

Statistical Analysis
Biostatistics
Leadership
Data Interpretation
Regulatory Interaction
Coaching and Mentorship

Education

M.S. or Ph.D. in Statistics
Degree in Biostatistics or related field

Tools

SAS

Job description

Senior or Principal Biostatistician – Leading CRO – Homebased – UK / Europe

We have recently partnered with an award-winning CRO, who are looking for an experienced Principal Statistician (or Senior looking to move into Principal), 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 clients.

Key Qualifications and Skills

  • M.S. or Ph.D. degree in statistics, biostatistics, or related field.
  • Experience in statistics, biostatistics or related field.
  • 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 competitors 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 likes to look at themselves more like an extended family with consideration of staff as individuals allowing a work-life balance.

Company culture:

This is a company where their people set them apart. Diverse teams enable them to become a better partner to their customers and help to fulfil our mission to advance and improve patients’ lives.

The company has an ‘Own It’ culture, driven by four key values that bring them together as individuals and set them apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. It is key to be a CRO that delivers excellence to their clients and to patients at every touchpoint. In short, to be the partner of choice in drug development.

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

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