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

ZipRecruiter; Altrincham; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading consultancy seeks a Senior Statistical Programmer to provide programming support across diverse projects in a collaborative environment. The role demands proficiency in SAS and includes responsibilities like leading meetings, performing data checks, and maintaining audit-ready documents. Candidates should have a BSc, MSc, or PhD in a numerical discipline and at least 4 years of relevant experience.

Benefits

Supportive management

Training and development opportunities

Friendly working environment

Qualifications

• 4+ years of relevant industry experience required.
• Experience in statistical programming and data management essential.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Lead internal and client study team meetings.
• Program and QC datasets and TFLs following specifications.

Skills

Statistical techniques

Programming in SAS

Data exploration

Quality control

Collaboration

Education

BSc, MSc, or PhD in numerical discipline

Job description

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
• Contribute to development of internal training materials
• Contribute to internal process improvement initiatives

Minimum Qualification Requirements

• 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.