Contract Senior / Principal Statistical Programmer - UK (Remote or Office Based)

Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work alongside Veramed. You will deliver high-impact programming solutions in an FSP-style capacity, across a range of projects and therapeutic areas. KEY RESPONSIBILITIES: The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs. TECHNICAL:

• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs.
• Author and review simple and complex study TFL shells.
• Author and review simple and complex dataset standards.
• Perform data checks and data exploration (e.g. using frequencies, histograms).
• Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice.
• Complete and review CDISC Validation tool reports.
• Ensure the appropriate standards are being applied and adhered to.
• Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival).
• Review of project management related documents.
• Maintain study master file documents and any other documents that are required to be audit ready.

• Lead internal and client study team meetings effectively.
• Present study updates internally and at client meetings.
• Share scientific, technical and practical knowledge within the team and with colleagues.
• Perform work in full compliance with applicable internal and client policies, procedures, processes and training.
• Build effective collaborative working relationships with internal and client team members.
• Seek opportunities to develop innovative ideas, sharing when appropriate.
• Mentorship of more junior team members.
• Contribution to development of internal training materials.
• Contribution to internal process improvement initiatives.

• BSc or above in numerical discipline (or relevant equivalent industry experience).
• At least 5 years of relevant industry experience.

• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs.
• Awareness of industry and project standards & ICH guidelines.
• Excellent verbal and written communication skills.
• Interpersonal/teamwork skills for effective interactions.
• Proficiency in data handling using SAS or other statistical software (e.g. R).
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
• Demonstrated problem solving ability and attention to detail.
• Ability to work independently and as part of a team.