Senior/Principal Programmer
Key Skills for This Role
Full Job Posting
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.
What you can expect
A warm, supportive and collaborative working environment.
An open-door management culture focused on development and progression.
Opportunities to own your role and shape your career path.
Exposure to a wide range of clients, studies and therapeutic areas within a unique CRO environment.
If you are passionate about delivering high-quality outputs, enjoy mentoring others, and want to make a genuine impact in a people‑focused organisation, we’d love to hear from you.
Veramed is a B Corp accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability.
As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.
About Veramed
Veramed is a biometrics CRO providing data management, biostatistics, and programming services to pharmaceutical and biotech sponsors.
Visit company websiteJobs and hiring trendsApply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
More jobs at Veramed
Principal Statistician/Manager Statistics for Consultancy Team
, USA
Senior Statistical Programmer (ADaM + R Prog)
, IND
Principal Statistical Programmer
, IND
Senior/ Principal Programmer (Macros/Standards)
, IND
Senior/Principal Statistician
, GBR
Principal Data Engineer (RWE)
, IND
Senior SDTM Programmer
, IND
Principal Statistician/Manager Statistics for Consultancy Team
, USA
DM Programmer
, GBR