Senior or Principal Statistical Programmer - Submissions
City of London, England, United Kingdom
Proclinical Staffing
Science or another 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 More ❯
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