Associate Director Statistical Programming - Oncology

JR United Kingdom; Birmingham; On-site; GBP 60,000 - 85,000; Full time

Job summary

A leading life science recruiter is seeking an Associate Director of Statistical Programming. This role involves overseeing programming teams, ensuring quality in output, and contributing to regulatory submissions, specifically in Oncology. Candidates should have a relevant degree and experience in statistical programming with a strong understanding of regulatory guidelines.

Qualifications

• Experience in Statistical Programming.
• Proficiency in SAS and understanding CDISC standards.
• Strong interpersonal skills and ability to work in teams.

Responsibilities

• Oversee creation of datasets, tables, and figures for studies.
• Manage internal and external programming teams.
• Review and validate SAS/R programs.

Skills

Statistical Programming

SAS

Oncology

Analytical Skills

Problem Solving

Communication

Education

Degree in Statistics, Mathematics, Computer Science, or related field

Job description

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Associate Director Statistical Programming - Oncology, birmingham

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Client:

Proclinical Staffing

Location:

birmingham, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Experienced in Statistical Programming and looking for your next step in your career?

Proclinical is seeking an experienced individual in Statistical Programming for an Associate Director position. This is a permanent position based in London, United Kingdom or Frankfurt, Germany.

Responsibilities:

• Oversee the creation of datasets, tables, listings, and figures for studies.
• Manage and oversee internal and external programming teams.
• Review, validate, and troubleshoot SAS/R programs.
• Ensure accuracy and perform quality control of outputs.
• Act as the primary programming contact for study teams.
• Collaborate with various departments to prepare submission-ready materials.
• Manage relationships with outsourced partners, including negotiations and audits.
• Monitor resource allocation and balance workload across studies.
• Develop standardized tools to improve efficiency.
• Train junior programmers and staff on best practices and regulatory updates.
• Support regulatory submissions with data packages and documentation.

Key Skills and Requirements:

• Degree in Statistics, Mathematics, Computer Science, or related field.
• Proficiency in statistical programming languages such as SAS.
• Understanding of global regulations and guidelines.
• Experience with clinical study data standards, particularly CDISC.
• Oncology and project management experience.
• Strong interpersonal and communication skills.
• Ability to work in a dynamic team environment.
• Strong analytical and problem-solving abilities.

If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at [emailprotected] .

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.

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