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

JR United Kingdom; London; Hybrid; GBP 50,000 - 80,000; Full time

Job summary

An exciting opportunity awaits for a Senior Statistical Programmer to join a forward-thinking consultancy in the UK. This role offers the flexibility of remote, office, or hybrid working arrangements, ensuring a work-life balance. You will be responsible for programming support across various projects, utilizing your expertise in SAS and statistical techniques. The company prides itself on fostering a supportive environment that encourages professional development and innovative thinking. Join a team that values collaboration and mentorship, where your contributions will directly impact the success of clinical trials and client relationships.

Benefits

Flexible working options

Training and support

Competitive package

Professional development opportunities

Unique company culture

Qualifications

• 4+ years of experience in statistical programming and clinical trials.
• Strong knowledge of SAS and statistical techniques.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Lead study team meetings and present updates to clients.
• Ensure compliance with regulations and mentor junior members.

Skills

SAS Programming

Statistical Techniques

Data Management

Clinical Trials

Team Leadership

Education

BSc in a numerical discipline

MSc in a numerical discipline

PhD in a numerical discipline

Tools

SAS

Job description

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Senior Statistical Programmer - UK (Remote/Office/Hybrid), London (City of London)

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Client:

Veramed

Location:

London (City of London), United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

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

We have an exciting opportunity for a Senior Statistical Programmer to join us on a permanent basis in the UK. We offer flexible working options, training, support, and a competitive package.

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

Key Responsibilities

Technical

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

General

• Lead study team meetings effectively
• Present study updates internally and to clients
• Share knowledge within the team
• Ensure compliance with regulations and policies
• Build collaborative relationships with teams
• Develop innovative ideas
• Mentor junior team members
• Contribute to training materials and process improvements

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, friendly working environment
• Opportunities for professional development
• A unique company culture focused on staff management and relationship building
• Ownership of your role and skill development