2 of 2 CDISC Jobs in the City of London

relevant field. Experience in SAS programming within the pharmaceutical industry. Understanding of clinical trial design and regulatory submissions. Familiarity with GCP and regulatory requirements. Knowledge of SDTM and ADaM CDISC standards. If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at h.hennigan@proclinical.com Apply Now: If you are interested in learning more More ❯

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 More ❯