Regulatory Clinical Trials Veeva Consultant

Full Job Description

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.