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

ZipRecruiter; Bolton; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

An exciting opportunity awaits for a Senior Statistical Programmer at a forward-thinking company. This role offers the chance to provide vital programming support across various projects in a collaborative environment. With a focus on quality and innovation, you will engage in meaningful work that contributes to the advancement of statistical analysis in clinical trials. The company fosters a warm and supportive atmosphere, encouraging personal and professional growth. If you are passionate about statistics and programming, this position is your chance to make a significant impact while developing your career in a unique CRO setting.

Benefits

Training and Support

Friendly Working Environment

Open-Door Management Policy

Career Development Opportunities

Qualifications

• 4+ years of relevant industry experience in statistical programming.
• Strong knowledge of clinical trial documents and statistical techniques.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Program and QC datasets and TFLs in SAS.

Skills

SAS Programming

Statistical Analysis

Data Exploration

Clinical Trial Documentation

Project Management

Education

BSc in a Numerical Discipline

MSc in a Numerical Discipline

PhD in a Numerical Discipline

Tools

CDISC Validation Tool

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 a Senior Statistical Programmer 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

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

General

1. Lead internal and client study team meetings effectively
2. Present study updates internally and at client meetings
3. Share scientific, technical, and practical knowledge within the team and with colleagues
4. Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
5. Build effective collaborative working relationships with internal and client team members
6. Seek opportunities to develop innovative ideas, sharing when appropriate
7. Line management or mentorship of more junior team members
8. Contribution to development of internal training materials
9. 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.