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Lead Biostatistician Oncology - Global Pharma

Proclinical Staffing

England

Remote

GBP 60,000 - 80,000

Full time

2 days ago
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Job summary

Join a leading life sciences recruiter as a Lead Biostatistician, contributing to oncology clinical trials from a remote location in London. You will oversee statistical activities and mentor a team, collaborating on impactful projects. Candidates should possess strong SAS and R skills, with experience in Phase II and III trials.

Qualifications

  • Proven experience in Phase II and III oncology trials.
  • Strong understanding of SAS and R.
  • Ability to work hands-on and adapt.

Responsibilities

  • Lead biostatistical activities for oncology clinical trials.
  • Collaborate with cross-functional teams for accurate analysis.
  • Mentor junior to mid-level programmers.

Skills

SAS
R
Leadership
Effective communication

Job description

Direct message the job poster from Proclinical Staffing

Director Clinical Operations and Biometrics, Global Biometrics SME

Ready to lead projects that bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!

Proclinical is seeking a Lead Biostatistician with a focus on oncology to permanently join our client's team. This role involves contributing to clinical trials, particularly in Phase II and III, and requires a strong background in biostatistics within the pharmaceutical industry. The position is remote-based in London, offering an opportunity to work on impactful projects in a dynamic environment.

This is a remote role based in London, the UK.

Responsibilities:

  • Lead and oversee biostatistical activities for oncology clinical trials.
  • Collaborate with cross-functional teams to ensure accurate statistical analysis and reporting.
  • Provide expertise in SAS and R, focusing on outputs and TFLs.
  • Engage and mentor junior to mid-level programmers to support project growth.
  • Address challenges related to candidate sourcing and engagement.

Key Skills and Requirements:

  • Proven experience in Phase II and III oncology trials.
  • Strong understanding of SAS and R, with oversight capabilities.
  • Ability to work hands-on and adapt to less structured environments.
  • Familiarity with statistical outputs and TFLs.
  • Effective communication and leadership skills to guide project teams.

If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at h.hennigan@proclinical.com.



Apply Now:

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.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Science
  • Industries
    Professional Services

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