Back
Metro location and strong pharma brand increase applicant density despite senior, niche clinical SAS skillset.
Clinical SDTM/ADaM standards and submission experience make cross-industry transfer difficult.
Mandatory 10+ years and specific SDTM/ADaM, SAS Viya, regulatory submission expertise enforce strict shortlisting.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Develop and validate SDTM and ADaM datasets including preparation of validation reports and submission packages.
Generate statistical tables, listings, safety figures, and interim analysis outputs for clinical studies.
Lead programming quality processes including review checklists, quality metrics, and support eCOA reconciliation and regulatory submissions.
10+ years of clinical SAS programming experience.
Strong expertise with SDTM and ADaM standards.
Hands-on experience with SAS, including SAS Viya for clinical programming.
Experience with Phase 1 PK studies and Phases 2–4 clinical trials across various therapeutic areas.
Experienced leader able to independently manage complex programming deliverables across multiple clinical phases.
Demonstrated capability in implementing and optimizing SAS Viya for clinical data workflows.
Ability to ensure compliance with industry regulatory standards and produce high-quality documentation for submissions.