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

JR United Kingdom; Ashton-under-Lyne; Remote; GBP 40,000 - 80,000; Full time

Job summary

An innovative consultancy is seeking a Senior Statistical Programmer to join their dynamic team in a flexible role. This position offers the chance to work on diverse projects while providing programming support across various therapeutic areas. With a strong emphasis on career growth and a collaborative culture, this role is perfect for someone eager to mentor others and contribute to process improvements. Enjoy a supportive environment that values knowledge sharing and professional development, making a significant impact in the field of clinical statistics.

Benefits

Flexible Working Arrangements

Training and Support

Career Development Opportunities

Unique Company Culture

Qualifications

• Minimum 4 years of relevant experience in statistical programming.
• BSc, MSc, or PhD in a numerical discipline or equivalent experience.

Responsibilities

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

Skills

SAS Programming

Statistical Techniques

Data Exploration

Clinical Trial Documentation

Education

BSc in Numerical Discipline

MSc in Numerical Discipline

PhD in Numerical Discipline

Job description

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Senior Statistical Programmer - UK (Remote/Office/Hybrid), Ashton-under-Lyne

Client:

Veramed

Location:

Ashton-under-Lyne, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

Job Views:

4

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

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

We are seeking a Senior Statistical Programmer for a permanent position 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

Technical

• Perform consistency reviews of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review study TFL shells and dataset standards
• Conduct data checks and exploration (e.g., frequencies, histograms)
• Program and QC datasets and TFLs in SAS following specifications and good practices
• Review CDISC Validation reports
• Ensure standards compliance
• Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis)
• Review project management documents
• Maintain audit-ready study documents

General

• Lead and present at study team meetings
• Share knowledge within the team and with clients
• Ensure compliance with regulations and policies
• Build collaborative relationships with team members
• Mentor junior staff and contribute to training materials
• Participate in process improvements

Minimum Qualifications

BSc, MSc, or PhD in a numerical discipline or equivalent industry experience; at least 4 years of relevant experience.

What To Expect

• A supportive and friendly working environment
• Development opportunities and career support
• Unique company culture focused on staff management and relationship building
• Opportunity to own your role and develop skills