Associate Director Statistical Programming - Oncology

JR United Kingdom; Kingston upon Hull; On-site; GBP 65,000 - 95,000; Full time

Job summary

A leading life sciences recruiter seeks an experienced Associate Director of Statistical Programming in Kingston upon Hull. This permanent role involves managing programming teams, ensuring data quality, and training junior staff within the oncology sector. The ideal candidate will have a degree in a quantitative field and be proficient in SAS.

Qualifications

• Experience with clinical study data standards, particularly CDISC.
• Oncology and project management experience.
• Ability to work in a dynamic team environment.

Responsibilities

• Oversee the creation of datasets, tables, listings, and figures for studies.
• Manage and oversee internal and external programming teams.
• Collaborate with various departments to prepare submission-ready materials.

Skills

Statistical programming

Interpersonal skills

Analytical abilities

Education

Degree in Statistics, Mathematics, Computer Science

Tools

SAS

Job description

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Associate Director Statistical Programming - Oncology, Kingston upon Hull, East Yorkshire

Client:

Proclinical Staffing

Location:

Kingston upon Hull, East Yorkshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

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 applying or have questions, please contact Heidi Hennigan at [emailprotected].

If interested, please click 'Apply' or request a callback at the top of this page to speak with one of our specialists.

Proclinical is a leading life sciences recruiter focused on connecting exceptional people with top positions globally. We act as an Employment Agency for this vacancy.

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