Senior Statistical Programmer - UK (Remote/Office/Hybrid)

JR United Kingdom; Greater Manchester; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

An innovative CRO is searching for a Senior Statistical Programmer to join their dynamic team in Greater Manchester. This role offers the flexibility of remote, office, or hybrid working arrangements, alongside a supportive environment that fosters career growth. You will be responsible for providing programming support across various projects, ensuring compliance with industry standards, and mentoring junior team members. With opportunities for professional development and a commitment to high-quality consultancy, this position is perfect for those looking to make a significant impact in the field of statistical programming.

Benefits

Flexible working arrangements

Professional development opportunities

Supportive working environment

Qualifications

• At least 4 years of relevant industry experience.
• BSc, MSc, or PhD in a numerical discipline.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Lead study team meetings and present updates.

Skills

SAS Programming

Statistical Techniques

Data Analysis

Clinical Trial Documentation

Education

BSc in Numerical Discipline

MSc in Numerical Discipline

PhD in Numerical Discipline

Tools

SAS

Job description

Social network you want to login/join with:

Senior Statistical Programmer - UK (Remote/Office/Hybrid), Greater Manchester

Client: Veramed

Location: Greater Manchester, UK

Job Category: Work abroad, Other

EU work permit required: Yes

Job Views:

8

Posted:

08.05.2025

Expiry Date:

22.06.2025

Job Description:

Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment that supports career growth.

We are seeking a Senior Statistical Programmer for a permanent role in the UK, offering flexible working arrangements, training, support, and a competitive package.

The role involves providing programming support across various projects, clients, and therapeutic areas.

Key Responsibilities

• Perform consistency reviews of clinical trial documents including protocols, SAPs, CRFs, CSRs.
• Author and review study TFL shells and dataset standards.
• Perform data checks and exploration using tools like frequencies and histograms.
• Program and QC datasets and TFLs in SAS following specifications and good practices.
• Review CDISC Validation reports and ensure standards compliance.
• Familiarity with basic statistical techniques such as t-test, ANOVA, regression, and survival analysis.
• Review project management documents and maintain audit-ready study files.

General Responsibilities

• Lead and participate in study team meetings and present updates.
• Share technical and scientific knowledge within the team.
• Ensure compliance with legislation, regulations, and company policies.
• Build collaborative relationships with team members and clients.
• Mentor junior team members and contribute to training materials and process improvements.

Minimum Qualifications

• BSc, MSc, or PhD in a numerical discipline or relevant industry experience.
• At least 4 years of relevant industry experience.

What to Expect

• A supportive and friendly working environment.
• Opportunities for professional development and career advancement.
• A unique CRO with innovative management and relationship-building approaches.

Please note: If you are not a passport holder of the country for the vacancy, a work permit may be required. For more information, check our blog.

Do not provide bank or payment details when applying. All applications should be made via the 'Apply now' button.

Created on 08/05/2025 by JR, United Kingdom