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

Veramed; West Midlands Combined Authority; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

Veramed offers a unique opportunity for Senior Statistical Programmers to provide programming support across various projects and therapeutic areas. The position promises a supportive working environment, where employee development is prioritized and industry standards are adhered to. With responsibilities spanning documentation review and team leadership, this role is ideal for those looking to advance their careers in a dynamic and innovative CRO.

Qualifications

• Minimum 4 years of relevant industry experience required.
• Familiarity with statistical analyses such as t-test, ANOVA, regression.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Author and review study TFL shells and dataset standards.
• Lead internal and client study team meetings.

Skills

Statistical techniques

Programming in SAS

Data exploration

Quality Control

Education

BSc, MSc, or PhD in a numerical discipline

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

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.