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2017-11-21 12:36:30
Veeva Integration Consultant at San Francisco 6 m contract MANAGERs COMMENTS:::: Veeva Integration w/ RIM with eCTD and eTMF attribute configuration experience is a WiNNER Responsibilities Participate in projects at life sciences R&D companies Preferred:: Rapidly configure and implement the Vault RIM suite (Vault Registrations, Vault Submissions, Vault Submissions Archive) which is used to manage regulatory affairs and regulatory operations content and data in the cloud Lead requirements workshops, design, prototype, configure and document content management/registration data solutions Perform project management tasks including resource planning, leading and motivating a cross-functional team, and project tracking and forecasting Ensure customer success from beginning to end of the engagement life cycle Requirements 1-4+ years of experience working with life sciences companies Experience implementing systems for life sciences as a consultant, business or IT representative for at least one of the following: Document or Data Management, Registration Tracking, eSubmissions, eCTD, XEVMPD, IDMP, Documentum, OpenText, SharePoint Proven ability to collaborate with diverse stakeholders and ensure delivery to a high degree of satisfaction Ability and willingness to â??roll up your sleevesâ? to design and implement a RIM solution Ability to communicate complex technical solutions to business users Quickly understand business requirements and create corresponding solution designs Nice to Have Understanding of global regulatory requirements, compliance considerations and processes for submission planning, submission content management, registration tracking, life sciences compliance, and/or computer systems validation Direct experience with systems such as Veeva Vault, PAREXEL/ LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, other regulatory information management or submission publishing systems, etc. Consulting experience Life Science, computer science or related degree preferred SaaS/Cloud experience
Key Skills:
Veeva Integration Consultant at San Francisco 6 m contract
2017-11-21 12:36:30
Job Type:
Contract
Veeva Integration Consultant at San Francisco 6 m contract MANAGERs COMMENTS:::: Veeva Integration w/ RIM with eCTD and eTMF attribute configuration experience is a WiNNER Responsibilities Participate in projects at life sciences R&D companies Preferred:: Rapidly configure and implement the Vault RIM suite (Vault Registrations, Vault Submissions, Vault Submissions Archive) which is used to manage regulatory affairs and regulatory operations content and data in the cloud Lead requirements workshops, design, prototype, configure and document content management/registration data solutions Perform project management tasks including resource planning, leading and motivating a cross-functional team, and project tracking and forecasting Ensure customer success from beginning to end of the engagement life cycle Requirements 1-4+ years of experience working with life sciences companies Experience implementing systems for life sciences as a consultant, business or IT representative for at least one of the following: Document or Data Management, Registration Tracking, eSubmissions, eCTD, XEVMPD, IDMP, Documentum, OpenText, SharePoint Proven ability to collaborate with diverse stakeholders and ensure delivery to a high degree of satisfaction Ability and willingness to â??roll up your sleevesâ? to design and implement a RIM solution Ability to communicate complex technical solutions to business users Quickly understand business requirements and create corresponding solution designs Nice to Have Understanding of global regulatory requirements, compliance considerations and processes for submission planning, submission content management, registration tracking, life sciences compliance, and/or computer systems validation Direct experience with systems such as Veeva Vault, PAREXEL/ LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, other regulatory information management or submission publishing systems, etc. Consulting experience Life Science, computer science or related degree preferred SaaS/Cloud experience
Key Skills:
