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Senior Statistical Programmer - UK

Warman O’Brien

United Kingdom

Remote

GBP 45,000 - 75,000

Full time

Yesterday
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Job summary

An independent CRO is seeking Senior Statistical Programmers to join their dynamic team remotely across the UK. This role offers the chance to lead statistical programming projects, ensuring high-quality deliverables while working with cutting-edge clinical research methodologies. With a focus on flexibility and a healthy work-life balance, this growing organization is dedicated to providing exceptional services to the pharmaceutical and biotechnology industries. If you are passionate about statistical programming and looking for an opportunity to advance your career in a supportive environment, this position is perfect for you.

Benefits

Flexible working hours
Healthy work-life balance
Fully remote position
Generous remuneration package

Qualifications

  • 6+ years of experience in statistical programming and clinical trials.
  • Master's or Bachelor's degree in relevant fields required.

Responsibilities

  • Lead statistical programming projects ensuring high-quality deliverables.
  • Develop and validate SDTM and ADaM datasets, ensuring compliance.

Skills

SAS
R
Statistical Programming
Data Structures
CDISC Compliance

Education

Master’s or Ph.D. in Statistics, Biostatistics, or Computer Sciences
Bachelor’s degree in Statistics, Biostatistics, or Computer Sciences

Tools

Define.xml
Macros

Job description

Senior Statistical Programmer | Independent CRO | Home Based | UK |

Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.

Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs, this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.

We’re seeking several Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK.

What you will be doing:

You’ll lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs.

What you will need:

  • A Master’s or Ph.D. degree in Statistics, Biostatistics or Computer Sciences and 6 years’ experience in statistical programming, OR a Bachelor’s degree in the above fields with at least 6 years’ experience in clinical trial statistical programming.
  • Excellent knowledge of SAS essential, with R advantageous.
  • Good working knowledge of data structures e.g. CDISC, SDTM, ADaM.
  • Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines.

What in it for you:

  • The opportunity to be involved in a growing organisation.
  • Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
  • Fully remote in the UK.
  • Generous remuneration package.

What to do next:

  • If this opportunity is of interest, please apply now with your CV as the organisation is looking to arrange interviews for the Senior Statistical Programmer as soon as possible.
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