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Consultant SAS, Clinical Data Management
Clinical Data Management (CDM), Medical Affairs
Serves as a technical specialist in the SAS application providing support to both CDM and Biostatistics at ApoPharma during the clinical drug development process. This includes but is not limited to the preparation, validation and maintenance of SAS programs and macros to generate SAS datasets, spreadsheets, ASCII files, data listings, tables and graphical displays of clinical trial data and safety data for ApoPharma products. May participate in the efforts for process improvement and technology upgrades regarding SAS technology. Works collaboratively with Clinical Data Management, Biostatisticians, Clinical Research, Medical Safety, Regulatory Affairs and Project Management at ApoPharma to meet project deliverables and timelines for clinical statistical programming and reporting.
28. Performs all work in support of our Corporate Values of Pride, Accountability, Integrity and Diligence; Demonstrates strong and visible support of our values.
29. Performs all work in accordance with all established regulatory and compliance and safety requirements.
30. All other duties as assigned.
· Proven SAS experience and expertise as demonstrated in previous work