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

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

Job summary

A leading company is seeking a Senior Statistical Programmer in Guildford, UK. This role offers a blend of home and office working, with a focus on programming and data analysis in clinical trials. You will be responsible for providing programming support across various projects while enjoying a supportive work environment that facilitates professional growth.

Benefits

Supportive management policy

Friendly working environment

Opportunities for personal and professional growth

Contribution to internal training materials

Qualifications

• At least 4 years of relevant industry experience required.

Responsibilities

• Perform consistency review of clinical trial documents.
• Lead internal and client study team meetings.
• Program and QC routine and ad hoc datasets in SAS.

Skills

Statistical Techniques

Programming in SAS

Data Management

Quality Control

Education

BSc, MSc, or PhD in a numerical discipline

Job description

Social network you want to login/join with:

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

Client: Veramed

Location: Guildford, United Kingdom

Job Category: Other

-

EU work permit required: Yes

Job Views:

4

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry-leading working environment with support and training for career growth.

We have an exciting opportunity for Senior Statistical Programmers to join us on a permanent basis in the UK. We can offer home and/or office working, training and support, and a competitive package.

The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients, and therapeutic areas.

Key Responsibilities

Technical

• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review simple and complex study TFL shells
• Author and review simple and complex dataset standards
• Perform data checks and data exploration (e.g., using frequencies, histograms)
• Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
• Complete and review CDISC Validation tool reports
• Ensure the appropriate standards are being applied and adhered to
• Familiarisation with simple statistical techniques (e.g., t-test, ANOVA, regression, standard survival)
• Review of project management related documents
• Maintain study master file documents and any other documents that are required to be audit ready

General

• Lead internal and client study team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical, and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
• Build effective collaborative working relationships with internal and client team members
• Seek opportunities to develop innovative ideas, sharing when appropriate
• Line management or mentorship of more junior team members
• Contribution to development of internal training materials
• Contribution to internal process improvement initiatives

Qualifications:

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

What To Expect

• A warm, friendly working environment in which to thrive both personally and professionally.
• A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
• A truly unique CRO that’s doing something different when it comes to managing staff, projects, and building relationships in the industry.
• The ability to own your role and develop your skills and experience.