Principal Statistician

Proclinical Group; City Of London; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading life sciences recruiter is seeking a Principal Biostatistician to work remotely and lead biostatistics programming activities for global studies. The role involves study design, statistical analysis, and regulatory submissions. Ideal candidates have an advanced degree in statistics, a strong grasp of statistical principles, and proficiency in SAS. Experience in regulatory submissions and mentoring is essential.

Qualifications

• Strong understanding of statistical principles and regulatory requirements.
• Ability to mentor and coach team members.
• Experience leading regulatory submissions.

Responsibilities

• Lead programming activities for a program of studies.
• Provide statistical input into study designs.
• Review database structures and data management coding conventions.
• Develop statistical analysis plans.
• Perform statistical analyses and report results.
• Support regulatory questions and labelling claims.
• Participate in client meetings and presentations.
• Contribute to research proposals and defense meetings.

Skills

Statistical principles

Experimental design

Communication skills

Project management

Proficiency in SAS

Education

Advanced degree in statistics or biostatistics

Tools

SAS

Job description

Work from anywhere and shape powerful biostatistics that drive results! Enjoy the freedom of remote work while making a global impact.

Proclinical is seeking a Principal Biostatistician to lead programming activities for a program of studies. This role involves contributing to study design, statistical analysis, and regulatory submissions while ensuring consistency and quality across projects. You will work in a collaborative environment, mentoring team members and supporting client interactions.

Responsibilities

• Lead biostatistics and programming activities for complex or high-value programs.
• Provide statistical input into study designs, including protocol development, sample size calculations, and randomization schemes.
• Review database structures, edit checks, and data management coding conventions.
• Develop statistical analysis plans, including defining derived data and designing tables, figures, and listings for clinical reports.
• Perform statistical analyses, interpret data, and report results.
• Write and review statistical methods sections of integrated study reports.
• Support responses to regulatory questions and contribute to labelling claims post-submission.
• Participate in client and investigator meetings, including presentations.
• Contribute to research proposals and participate in proposal defense meetings.
• Mentor and coach team members to foster professional growth.

Key Skills and Requirements

• Advanced degree in statistics, biostatistics, or a related field.
• Strong understanding of statistical principles, experimental design, and regulatory requirements.
• Proficiency in statistical software packages, particularly SAS.
• Experience leading regulatory submissions.
• Excellent communication, interpersonal, and project management skills.
• Ability to translate client needs into statistical practices and educate stakeholders on statistical concepts.

If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at [e-mail].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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