Associate Director Statistical Programming - Oncology

TN United Kingdom; London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking an Associate Director in Statistical Programming to lead teams and oversee the creation of datasets for oncology studies. This permanent role offers the opportunity to manage both internal and external programming teams, ensuring quality control and compliance with global regulations. Ideal candidates will have a strong background in statistical programming, particularly with SAS, and possess excellent communication and project management skills. Join a dynamic team environment where your expertise will contribute to impactful clinical trials and innovative healthcare solutions.

Qualifications

• Experienced in statistical programming with a focus on oncology.
• Proficient in SAS and understanding of clinical study data standards.

Responsibilities

• Oversee creation of datasets and figures for studies.
• Manage programming teams and ensure output quality.
• Collaborate with departments for submission-ready materials.

Skills

Statistical Programming

SAS

Project Management

Analytical Skills

Communication Skills

Education

Degree in Statistics

Degree in Mathematics

Degree in Computer Science

Job description

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Associate Director Statistical Programming - Oncology, London

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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:

6aa44f51552f

Job Views:

3

Posted:

10.05.2025

Expiry Date:

24.06.2025

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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.