Regulatory Clinical Trials Veeva Consultant
4 weeks ago
Regulatory Clinical Trials Veeva Consultant
Onsite at Tarrytown, NY 10591
Full Time OR 12 Months Contract
It's a Banking Client.
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.
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