Associate Specialist, Clinical Data Management, Hybrid
Full-time
Merck & Co.
Job DescriptionAssumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva platforms along with the external data captured in support of the clinical studies.--Coordinates and participates in the following activities: Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management (GCDM), Clinical Research (CR) and Global Safety (GS).- Review the technical
Vacancy posted 4 hours ago
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