Groton, CT, USA
12 days ago
IT - Principal Consultant | LifeSciences | Clinical Trials, Compliance & Safety
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Detailed Job Description:

Masters Degree (Pharma, Life sciences or equivalent) with Minimum 4-6 Years of Experience or Bachelor s degree or foreign equivalent with Minimum 8 Years of experience required. Experience in the full System Development Life Cycle (SDLC) on a variety of technologies and platforms preferably in pharma IT space Must be able to translate business requirements into well-formed technical and system requirements. Experience with modeling business processes, data flows, and workflow processes depicting relationships between Clinical data entities. Strong business consulting skills associated with complex IT system implementation spanning over 12-18 months. Strong oral & written communication skills, Business stakeholder management Must have performed business requirement analysis, use case modeling from a business analysis/consulting standpoint. At least 4-6 Years experience in one or more of the following skills is a must Clinical Trial Supply Chain and Inventory management with understanding of Clinical Material Requirement Planning (MRP), Clinical Inventory, Clinical Forecasting, Clinical Packaging, Clinical Labeling, Clinical Distribution, Clinical Depots, Clinical sites, IRT/IVRS and Clinical Trial Management System

Minimum years of experience*: 9

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