Senior/Principal Programmer
Veramed Limited · United Kingdom · posted 10 days ago
Going rate £54,700UK median £56,914
Home Office going rates from
Occupation
2134Programmers and software development professionals
Going rate for this occupation: £54,700 · UK median pay £56,914
Home Office going rates from
Where this salary sits
- UK pay for this occupation
- This role£68,242 to £102,860estimated
- Going rate£54,700
- UK median£56,914
View these figures as a table
| Percentile | Pay |
|---|---|
| 10th | £32,835 |
| 25th | £42,289 |
| 50th | £56,914 |
| 75th | £75,794 |
| 90th | £102,860 |
| Going rate | £54,700 |
| UK median | £56,914 |
Sponsorship
Sponsorship chance
Very high
- Licensed for Skilled Worker
- Occupation is eligible for Skilled Worker
- Estimated salary clears the going rate
On the public records we hold, sponsorship for this role looks likely: licensed for Skilled Worker, and occupation is eligible for Skilled Worker.
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We have an exciting opportunity for a Senior or Principal Statistical Programmer with strong SAS experience (and R exposure advantageous) to join Veramed on a permanent basis in the UK. We offer flexible home and/or office working, best‑in‑class training, and a competitive total reward package.
The primary purpose of this role is to provide high-quality programming support to the statistics and programming department across a broad range of projects, clients and therapeutic areas. At Senior and Principal level, you will play a key role in ensuring technical excellence, with scope to take on leadership, mentoring and project responsibilities depending on experience. At Principal level, the role may also include technical leadership, strategic input, line management and process improvement initiatives.
Key Responsibilities
Technical:
Review clinical trial documentation including protocols, SAPs, CRFs and CSRs.
Author, review and approve TFL shells and dataset specifications.
Develop, validate, review and document SAS programs for datasets, TFLs and macros in line with best programming practices.
Identify data issues, trends and outliers, and resolve or escalate as appropriate.
Complete, review and approve CDISC validation tool outputs.
Maintain awareness of emerging standards and assess their impact on ongoing and future studies.
Ensure study documentation is audit-ready, including maintenance of the study master file.
Maintain and develop technical expertise in SAS; stay informed of industry and regulatory developments.
Leadership & Collaboration:
Lead and contribute effectively to internal, client, study and cross-functional meetings.
Present study updates internally and to clients.
Share scientific, technical and practical knowledge across teams.
Support and mentor colleagues; contribute to internal technical training where appropriate.
Drive continuous improvement initiatives across programming processes.
Build strong, collaborative relationships with internal and client stakeholders.
Ensure all work is delivered in compliance with applicable SOPs, policies and training requirements.
Minimum Requirements:
BSc, MSc or PhD in a numerical or scientific discipline (or equivalent industry experience).
At least 4 years’ relevant industry experience in statistical programming.
Strong understanding of the clinical drug development process, including study designs, endpoints and disease areas.
Information from public records, not immigration advice.