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

ZipRecruiter; Bury; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

An innovative CRO is seeking a Senior Statistical Programmer to enhance their statistics and programming department. This role offers a unique opportunity to work in a warm and friendly environment, providing programming support across various projects and therapeutic areas. You will engage in data exploration, lead team meetings, and mentor junior members while ensuring compliance with industry standards. With a focus on career growth, this position allows you to own your role and develop your skills in a supportive setting. Join a forward-thinking organization that values your contributions and fosters professional development.

Benefits

Training and Support

Open-Door Management Policy

Friendly Working Environment

Career Progression Opportunities

Qualifications

• 4+ years of experience in statistical programming and clinical trials.
• Strong knowledge of SAS programming and statistical techniques.

Responsibilities

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

Skills

SAS Programming

Statistical Techniques

Data Exploration

Project Management

Education

BSc in Numerical Discipline

MSc in Numerical Discipline

PhD in 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 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, and 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. Familiarize with simple statistical techniques (e.g., t-test, ANOVA, regression, standard survival).
9. Review project management related documents.
10. Maintain study master file documents and other documents 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. Mentor and line manage junior team members.
8. Contribute to the development of internal training materials.
9. Contribute to internal process improvement initiatives.

Minimum Qualification Requirements

1. BSc, MSc, or PhD in a numerical discipline (or relevant industry experience).
2. At least 4 years of relevant industry experience.

What To Expect

• A warm, friendly working environment to thrive both personally and professionally.
• A supportive, open-door management policy to aid in your development and career progression.
• A unique CRO that manages staff, projects, and relationships innovatively.
• The opportunity to own your role and develop your skills and experience.