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 jon.gibbs@veramed.co.uk or via LinkedIn.