Strategic Principal Biostatistician - Clinical Trial Leader in London

Strategic Principal Biostatistician - Clinical Trial Leader in London

London Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Warman O'Brien

At a Glance

  • Tasks: Manage clinical trial programs and provide statistical oversight on drug development projects.
  • Company: Warman O'Brien is a recruitment firm focused on the life sciences sector in the UK.
  • Benefits: Candidates can expect opportunities for coaching and professional development.
  • Other info: Interested applicants can reach out via email for more details.
  • Why this job: Join a dynamic team leading drug development projects in a pivotal role.
  • Qualifications: A Ph.D. or Master's degree in statistical science or related fields is required.

The predicted salary is between 60000 - 80000 £ per year.

Warman O'Brien is seeking biostatisticians to join their team in the UK. The role involves managing clinical trial programs and providing statistical oversight on drug development projects. Candidates should possess a Ph.D. or Master's degree in statistical science or related fields.

Responsibilities include:

  • Coaching junior biostatisticians
  • Writing statistical reports
  • Ensuring compliance with regulatory requirements

Interested applicants can reach out via email at aimee@warmanobrien.com for more details.

Strategic Principal Biostatistician - Clinical Trial Leader in London employer: Warman O'Brien

Warman O'Brien offers a unique opportunity to work in the UK’s life sciences sector, focusing on clinical trials. The team values professional growth, providing coaching for junior biostatisticians. Join us to make a significant impact in drug development.

Warman O'Brien

Contact Details:

Warman O'Brien Recruitment Team

We think you need these skills to ace Strategic Principal Biostatistician - Clinical Trial Leader in London

Ph.D. or Master's degree in statistical science
Clinical Trial Management
Statistical Oversight
Coaching and Mentoring
Statistical Reporting
Regulatory Compliance
Drug Development Knowledge