Associate Director Statistical Programming - Oncology

Proclinical Group; London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is on the lookout for an experienced Statistical Programmer to step into an Associate Director role. This permanent position offers an exciting opportunity to lead programming efforts, manage teams, and ensure the accuracy of study outputs. The role involves collaboration with various departments and external partners, enhancing efficiency through standardized tools, and mentoring junior staff. If you're ready to take your career to the next level in a dynamic environment, this is the perfect opportunity for you.

Qualifications

• Experience in statistical programming with a focus on SAS.
• Strong understanding of clinical study data standards, particularly CDISC.

Responsibilities

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

Skills

SAS

Statistical Programming

Analytical Skills

Project Management

Interpersonal Skills

Problem-Solving

Education

Degree in Statistics

Degree in Mathematics

Degree in Computer Science

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 [e-mail].

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.

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