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

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

Job summary

Veramed is seeking a Senior Statistical Programmer to join their team in the UK, offering remote, office, or hybrid working options. The role involves providing programming support across various projects, ensuring compliance with standards, and contributing to team development. Candidates should have a strong background in statistics and programming, with a minimum of 4 years of relevant experience.

Benefits

Supportive management policy

Warm working environment

Opportunities for career advancement

Qualifications

• At least 4 years of relevant industry experience.
• Familiarisation with statistical techniques such as t-test, ANOVA, regression.
• Experience in leading internal and client study team meetings.

Responsibilities

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

Skills

Programming in SAS

Data checks

Statistical techniques

Collaboration

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

1 month ago Be among the first 25 applicants

Direct message the job poster from Veramed

Principal Talent Acquisition Consultant at Veramed

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

1. Technical
2. Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
3. Author and review simple and complex study TFL shells
4. Author and review simple and complex dataset standards
5. Perform data checks and data exploration (e.g., using frequencies, histograms)
6. Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
7. Complete and review CDISC Validation tool reports
8. Ensure the appropriate standards are being applied and adhered to
9. Familiarisation with simple statistical techniques (e.g., t-test, ANOVA, regression, standard survival)
10. Review of project management related documents
11. Maintain study master file documents and any other documents that are required to be audit ready
12. General
13. Lead internal and client study team meetings effectively
14. Present study updates internally and at client meetings
15. Share scientific, technical, and practical knowledge within the team and with colleagues
16. Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
17. Build effective collaborative working relationships with internal and client team members
18. Seek opportunities to develop innovative ideas, sharing when appropriate
19. Line management or mentorship of more junior team members
20. Contribution to development of internal training materials
21. Contribution to internal process improvement initiatives
22. BSc, MSc, or PhD in a numerical discipline (or relevant equivalent industry experience)
23. 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 your development and tools to advance your career.
• A unique CRO that manages staff, projects, and relationships differently.
• The opportunity to own your role and develop your skills and experience.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research

Industries

• Pharmaceutical Manufacturing, Health and Human Services, and Research Services