We have a unique combination of information systems and project management skills. Experts in delivery of validated, submission quality clinical data. Extensive experience in development and validation of clinical reporting systems.

Consultant to major pharmaceutical organizations. Projects include UNIX and SAS system development of automated analysis dataset creation system, key member of global standards definition team working on CDISC compliant standards for clinical development. Mapped legacy neurological data to SDTM standard for submission to CAMD industry intitaitve. Validation of submission tables and datasets. Provide clinical programming support for Oncology and Neurology trials at major pharmaceutical companies. Key member of rapid response programming team generating adhoc support for Nuerologic Regulatory Submissions and Phase 4 oncology clinical group. Working in UNIX and Windows environment supporting SAS programming.

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