Design Experience in Large Complex Multi-terabyte data environments & ability to translate business requirements into functional requirements documentation or work with light requirements in iterative fashion.
Perform sourcing and category management responsibilities for a specific sub-category of spend, including stakeholder engagement, competitive bidding and supplier monitoring, while delivering supply market intelligence and insights to sourcing managers via active management of external subscriptions and services.
Participate in design reviews and provide input to the design recommendations. Incorporate security requirements into design; and provide input to information/data flow, and understand and comply with Project Life Cycle Methodology in all planning steps.
In this role, the selected candidate will be responsible for the E-Clinical Platform software solutions including Siebel CTMS, Mobile CRA, Clinical Development Analytics, Argus Pharmacovigilence & Safety, Life Sciences Data Hub, Clear Trial and InForm EDC.