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

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

Job summary

An innovative CRO is seeking a Senior Statistical Programmer to join their dynamic team in the UK. This role offers the flexibility of remote, office, or hybrid work arrangements, and emphasizes personal and professional growth. You will be responsible for programming support across various projects, ensuring compliance with standards, and mentoring junior members. The company fosters a supportive environment with an open-door management policy, encouraging collaborative relationships and innovative contributions. If you're passionate about statistics and programming, this is an exciting opportunity to make a significant impact in the field.

Benefits

Training and support

Friendly working environment

Open-door management policy

Opportunities for skill development

Qualifications

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

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Lead internal and client study meetings.

Skills

SAS Programming

Clinical Trial Documentation

Statistical Techniques

Data Checks and Exploration

Project Management

Education

BSc in a relevant numerical discipline

MSc in a relevant numerical discipline

PhD in a relevant numerical discipline

Tools

CDISC Standards

Job description

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Senior Statistical Programmer - UK (Remote/Office/Hybrid), United Kingdom

Client:

Veramed

Location:

United Kingdom

Job Category:

Other

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 that supports career growth.

We are offering a permanent position for a Senior Statistical Programmer in the UK, with options for home, office, or hybrid work, along with training, support, and a competitive package.

The role involves providing programming support across various projects, clients, and therapeutic areas within the statistics and programming department.

Key Responsibilities

Technical

• 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 (e.g., frequencies, histograms)
• Program and QC datasets and TFLs in SAS following specifications and good programming practices
• Complete and review CDISC Validation reports
• Ensure standards compliance
• Familiarity 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 and facilitate internal and client study meetings
• Present study updates internally and externally
• Share technical and scientific knowledge within the team
• Ensure compliance with applicable regulations and policies
• Build collaborative relationships with team members and clients
• Contribute to innovative ideas and internal training materials
• Mentor junior team members
• Participate in process improvement initiatives

Qualifications:

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

What To Expect

• A supportive, friendly working environment for personal and professional growth
• Open-door management policy to aid development
• A unique CRO with a different approach to staff and project management
• Opportunities to own your role and develop skills