Lead Biostatistician Oncology - Global Pharma

Proclinical; London; Remote; GBP 70,000 - 90,000; Full time

Job summary

A leading company in pharmaceutical innovation is seeking a Lead Biostatistician focusing on oncology to join their team in London. This remote role offers the opportunity to lead biostatistical activities for impactful clinical trials. Ideal candidates will have proven experience in Phase II and III trials, strong SAS and R skills, and the ability to mentor junior staff.

Qualifications

• Proven experience in Phase II and III oncology trials.
• Strong understanding of SAS and R, with oversight capabilities.
• Effective communication and leadership skills.

Responsibilities

• Lead and oversee biostatistical activities for oncology clinical trials.
• Collaborate with cross-functional teams to ensure accurate statistical analysis and reporting.
• Engage and mentor junior to mid-level programmers.

Skills

SAS

R

Project Leadership

Statistical Outputs

Effective Communication

Job description

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Client:

Proclinical

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

16cc1371d148

Job Views:

7

Posted:

25.06.2025

Expiry Date:

09.08.2025

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Job Description:

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.