of experience in clinical data standards, data management, or programming within pharma/biotech/clinical research. * 2–3 years... of clinical data interoperability frameworks and submission standards. * Strong Expertise in CDISC standards (SDTM, ADaM...
workflows with regulatory and industry standards. Required Qualifications 5–7 years of experience in clinical data standards..., data management, or programming within pharma/biotech/clinical research. 2–3 years of hands-on experience with USDM...