Onsite - DATA ARCHITECT, Unified Regulatory Platform in Raritan, NJ - Strong & Recent Pharmaceutical Background
VINEET SHARMA
Please share resume to Vin...@vbeyond.com
15+ Years total experienced profile required
7+ years’ experience as a data architect in Pharmaceutical R&D
SUMMARY –
The client is looking for a senior-level Data Architect who has strong experience in the pharmaceutical R&D domain, especially with regulatory data. This person will work onsite in Raritan, NJ, partnering with business and technical teams to design data architecture for a Unified Regulatory Platform. The role requires someone who understands structured and unstructured data, can map data flows, ensure data quality, and align with data governance standards. Experience with Veeva Vault RIM, Snowflake or Denodo, and product master data is a big plus. In short, they need a hands-on data expert with a pharma industry background who can help clean up, integrate, and organize complex regulatory data to support digital transformation.
Position: Data Architect, Unified Regulatory Platform
Location - Raritan, NJ - Onsite
Duration: 3-6 Months
Responsibilities:
Client is seeking an experienced Data Architect to support our Unified Regulatory Platform program working out of the NJ
Roles and Responsibilities:
• Partner with Regulatory subject matter experts, implementation
and service partners, and product and platform technical owners and engineers
to design scalable, extensible and supportable data architectures that drive
business value in support of the Unified Regulatory Platform Strategy and Digital Transformation
Strategy.
• Develop data architecture artifacts in collaboration with key
stakeholders using Client standard tooling: Data Flow Diagrams, Entity
Relationship Diagrams, Data Integration Artifacts, etc.
• Responsible for architecture alignment to Regulatory, R&D,
Client Innovative Medicine and Client Enterprise data and data
platform strategies, patterns and standards.
• Identify data that will need to be integrated across Regulatory
solutions and its authoritative source.
• Advocate for data-driven decision-making by providing insights
and recommendations based on data analysis and architecture principles.
• Serve as a coach to business and IT product team partners to
shape strategy through sharing expertise in data governance, data quality, and
data integration best practices.
• Proactively identify opportunities for leveraging data as an
asset to enhance business capabilities and drive competitive advantage.
• Ability to communicate and collaborate effectively on the topics
of pharmaceutical product registrations and IDMP, Regulatory submission content
management, Submission Planning, Submission Publishing, Submission Archival,
Labeling and Health Authority Interactions.
2025 Deliverables:
• Partner with Regulatory Data Office to define procedures and
processes to harmonize, standardize and remediate data in preparation for URP
migration (data cleanup/remediation in place, transformation rules on
migration, etc).
• Support Regulatory product mastering efforts (including relevant
reference data) – map critical URP data and document objects in Lean IX and
Erwin
• Develop data flow diagrams as requested (both Regulatory domain
and boundary functions and processes)
• Drive alignment between URP, Regulatory, sector and enterprise
governance frameworks, including policies for the creation, maintenance and
stewardship of master data, reference data and critical data elements.
• Map data lineage for URP product master data and upstream and
downstream relationships to other Regulatory domain and cross-domain solutions
(upstream and downstream)
• Partner with the Regulatory Data Hub technical product owner and
architect on ingestion and transformation/refactoring of core operational data
and content coming from URP to support upstream, downstream, analytics and data
science use cases going forward.
• Support critical path URP data profiling and governance requests
as requested
• Support data office in helping to align emergent/overlapping
data-driven initiatives (ePI/eLabeling and IDMP) to Regulatory and URP data
strategy
Experience:
• 7 years’ experience as a data architect in Pharmaceutical
R&D
• 7 years’ experience working with structured and unstructured
data (for example, content)
• Product Master Data Management experience preferred
• Experience with Veeva Vault RIM and Vault platform APIs
preferred
• Experience working with Snowflake and/or Denodo preferred
Education:
• BA/BS degree in a technical, engineering or scientific field
• AWS Data Engineer Certification (or Azure/GCP equivalent)
preferred
Thanks & Regards,
Vineet Kumar Sharma
Senior Recruitment Executive - (US Operations)
Email: Vin...@vbeyond.com
LinkedIn: linkedin.com/in/vineetrpo
VBeyond Corporation (USA | UK | CANADA | INDIA)
www.vbeyond.com | New Jersey, USA
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VINEET SHARMA
15+ Years total experienced profile required
7+ years’ experience as a data architect in Pharmaceutical R&D
SUMMARY –
The client is looking for a senior-level Data Architect who has strong experience in the pharmaceutical R&D domain, especially with regulatory data. This person will work onsite in Raritan, NJ, partnering with business and technical teams to design data architecture for a Unified Regulatory Platform. The role requires someone who understands structured and unstructured data, can map data flows, ensure data quality, and align with data governance standards. Experience with Veeva Vault RIM, Snowflake or Denodo, and product master data is a big plus. In short, they need a hands-on data expert with pharma industry background who can help clean up, integrate, and organize complex regulatory data to support digital transformation.