Contract Senior / Principal Statistical Programmer - UK (Remote)

Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work alongside Veramed.

Do you have any of the following skillsets? if so, please reached out detailing your experience:

• PK Programming expertise - strong NONMEM and Pop PK expertise
• Disclosure & Anonymisation - knowledge and awareness of disclosure and/or anonymisation with experience programming in support of clinical trial disclosures (ex. Preparing uploads to clintrial.gov, etc.). Uses CSR data and tables to prepare. Experience applying data anonymisation rules to study data.
• ISS/ISE experience - hands on experience ISS/ISE data pooling.

ADDITIONAL REQUIREMENTS:

• 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.

Please use the link to apply or if you wanted to have a chat feel free to reach out to me at [email protected] or via LinkedIn.