| Senior Regulatory Clinical Trials Architect with Veeva Experience at Remote, Remote, USA |
| Email: [email protected] |
| From: james, rwaltz [email protected] Reply to: [email protected] Onsite at Tarrytown, NY 10591 Full Time OR 12 Months Contract Looking for 15 yrs overall experience Main Skills: Veeva vault platform Gxp and non Gxp Key responsibilities: Experience working with Regulatory and Quality area in Clinical trials. Experience in leading system design as per Business requirement and add non-functional requirement as needed. Lead Solution reviews for the project and get it approved from review board. Familiarity with Architecture Frameworks/Processes (e.g. TOGAF) and help define patterns and other architectural accelerators. Experience in IT architecture, infrastructure, and cloud development. System experience managing architecture of complex cross-functional systems. Strong knowledge of SDLC methodologies. Required skills: Must have Veeva vault platform (Veeva RIM, Veeva Submissions, Archive, QMS, Quality Docs) experience. Experience in Architecture Design for regulatory and quality Gxp and non Gxp IT systems. Good to have skills: Good problem solving, technical writing and verbal communication skills. Understands system and data security. Other important details: Extensive experience in large clinical trials. Understands the complete life cycle of clinical trials. Proved and extensive efficiency data analytics and data mapping experience. Be a SME that can guide the internal teams. Keywords: information technology New York |
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| Fri Jan 19 03:13:00 UTC 2024 |