Senior Principal Biostatistician

Psiweb; Greater London; On-site; GBP 70,000 - GBP 90,000; Full time

Job summary

A leading biotechnology company in the United Kingdom seeks a Senior Principal Biostatistician to lead statistical tasks for clinical trials. In this role, you will develop statistical analysis plans, collaborate cross-functionally, and implement innovative trial designs. The ideal candidate should have a PhD or MS with extensive experience, strong communication skills, and fluency in English. Join a passionate team dedicated to advanced quantitative sciences and drive decision-making in clinical trials.

Qualifications

• PhD experience preferred or MS with extensive experience.
• Fluent in English (oral and written).
• Strong communication and presentation skills.

Responsibilities

• Responsible for all statistical tasks on the assigned trials.
• Develop statistical analysis plans and reporting activities.
• Collaborate with cross-functional teams for quality deliverables.
• Drive quantitative decision making in assigned programs.

Skills

Statistical models

Data exploration methodologies

Communication skills

Presentation skills

Education

PhD or MS with extensive experience

Job description

Summary

We are in search of a Senior Principal Biostatistician to join a passionate team within Advanced Quantitative Sciences – Full Development, Neuroscience. Come to an industry leader where you will lead implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners

Office Location: London (The Westworks).

About the role

Key Responsibilities

• Responsible for all statistical tasks on the assigned trials.
• Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
• Contribute to planning and execution of exploratory analyses and statistical consultation within your cross-functional teams.
• Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
• Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
• Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
• Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings

Role Requirements

• PhD experience preferred OR MS with extensive experience
• Fluent English (oral and written)
• Strong communication and presentation skills

How to Apply

To find out more and apply, please click here .