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Lead Statistician

TN United Kingdom

United Kingdom

Remote

GBP 50,000 - 90,000

Full time

Today
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Job summary

An established industry player is seeking a Lead Statistician to enhance their early development statistics function. In this pivotal role, you'll oversee statistical input for clinical trials, collaborating with international regulatory bodies while managing a dedicated team of statisticians. Your expertise will be crucial in ensuring the integrity of statistical analyses and in representing the company at global conferences. This is an exciting opportunity to make a significant impact in the pharmaceutical sector, where your contributions will drive innovation and regulatory compliance.

Qualifications

  • Over 5 years of experience in clinical trial studies in the Pharmaceutical industry.
  • Experience leading statistical oversight on clinical studies.

Responsibilities

  • Provide statistical input and advice on studies across therapeutic areas.
  • Collaborate with international regulatory bodies and manage a small team.

Skills

Statistical Analysis
Clinical Trials
Team Management
Collaboration with Regulatory Bodies

Education

MSc in Biostatistics
MSc in Statistics

Job description

Role Overview


We are currently supporting a global pharmaceutical company, with their search for a Lead Statistician to support their early development statistics function.

As a Lead Statistician for this business, you will oversee a key function within the business and act as the key point of contact for vendors and CRO’s.

Your role will involve providing key statistical input, collaborating with international drug regulatory bodies as well as acting as a global key representative for this pharmaceutical business.

Key Duties and Responsibilities


1.Offer key statistical input/advice on studies, across one or more therapeutic area.

2.Collaborate with international regulatory bodies.

3.Manage junior/a small team of statisticians.

4.Partake in global conferences and act as subject matter expert.

Role Requirements


1.A MSc of above in Biostatistics, Statistics or a similar degree

2.At-least five years’ experience working on clinical trial studies within the Pharmaceutical/CRO/Medical Device industry.

3.Experience leading studies/oversight for statistical aspects on a clinical study.

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.

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Created on 26/04/2025 by TN United Kingdom

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