Provide product feedback to sales and marketing including customer feedback on product enhancements, service and policies through direct feedback as well as demonstration assessments and competitive developments.
Manage projects as they relate to Pfizers Clinical Data Management Systems (CDMS). Analyze multiple models/systems to ensure data integrity and documented, defensible collection/management of these data. Partner with global Clinical Trial Process Quality (CTPQ) regarding process across models.
The clinical documentation improvement department is part of clinical informatics. This department provides the opportunity to learn new skills, new software, and work closely with physicians, informaticists and coders.
Evaluate and review data and study analytical reports and assay validation reports, as appropriate, to ensure laboratories are performing analysis in compliance with current regulatory, industry, and Pfizer standards and that data are meeting regulatory and scientific requirements.