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.
GENERAL: 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.
MINIMUM QUALIFICATION REQUIREMENTS: BSc or above in numerical discipline (or relevant equivalent industry experience).
At least 5 years of relevant industry experience.
ADDITIONAL REQUIREMENTS: 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.
Please use the link to apply or if you wanted to have a chat feel free to reach out to me at or via LinkedIn.