Pharmaceutical DATA ARCHITECT, Unified Regulatory Platform in Raritan, NJ – Day 1 Onsite

Please share resume to VineetS@vbeyond.com

Rate: $78/hr. C2C

Implementation: Birlasoft

The client is looking for a Data Architect with 7+ years of experience in pharmaceutical R&D, specifically in regulatory domains like product registrations, IDMP, submission management, and labeling.

The role supports the Unified Regulatory Platform (URP), so hands-on experience in data governance, data lineage, master/reference data management, and data migration/remediation is key.

Must have strong skills in data architecture design (data flow diagrams, ERDs, integration), and experience with tools like Veeva Vault RIM, LeanIX, Erwin, and platforms like Snowflake or Denodo.

Familiarity with structured/unstructured data, compliance frameworks (e.g., FDA, IDMP), and preferably AWS/Azure/GCP certification is highly desired.

The client wants someone who can align data strategy with business goals and support ongoing regulatory transformation efforts.

Position: Data Architect, Unified Regulatory Platform

Location: Raritan, NJ – Day 1 Onsite

Duration: 6 Months (with possibility of extension)

Client is seeking an experienced Data Architect to support our Unified Regulatory Platform program working out of the NJ

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 of experience as a data architect in Pharmaceutical R&D
• 7 years of 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: VineetS@vbeyond.com

LinkedIn: linkedin.com/in/vineetrpo

VBeyond Corporation (USA | UK | CANADA | INDIA)

www.vbeyond.com | New Jersey, USA

Note – VBeyond is fully committed to Diversity and Equal Employment Opportunity.

Disclaimer: We respect your Online Privacy. This is not an unsolicited mail. Under Bill S 1618 Title III passed by the 105th US Congress this mail cannot be considered Spam as long as we include Contact information and a method to be removed from our mailing list. If you are not interested in receiving our e-mails, then please reply to VineetS@vbeyond.com subject=Remove. Also mention all the e-mail addresses to be removed which might be diverting the e-mails to you. We are sorry for the inconvenience.