Samniya Avionics Techsys Pvt.Ltd.
Data Architect – Regulatory & Compliance
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Data Architect – Regulatory & Compliance with a contract length of over 6 months, offering a pay rate of $101,654.56 - $130,000 per year. Key skills include IDMP experience, data modeling, ETL design, and SQL proficiency.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
590
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🗓️ - Date
October 22, 2025
🕒 - Duration
More than 6 months
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🏝️ - Location
On-site
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📄 - Contract
Unknown
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🔒 - Security
Unknown
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📍 - Location detailed
Raritan, NJ 08869
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🧠 - Skills detailed
#Cloud #Data Modeling #Data Management #Security #Azure Data Factory #Data Quality #Data Pipeline #Azure #Business Analysis #Documentation #Data Integration #Informatica #MDM (Master Data Management) #SQL (Structured Query Language) #Data Governance #Talend #Metadata #ADF (Azure Data Factory) #Compliance #Data Documentation #Data Engineering #AWS (Amazon Web Services) #Data Privacy #Data Architecture #"ETL (Extract #Transform #Load)"
Role description
Job Overview:
We are looking for a highly skilled Data Architect with strong experience in Regulatory, Compliance, and IDMP (Identification of Medicinal Products) domains. The ideal candidate will design and manage enterprise data models, regulatory data pipelines, and integration frameworks supporting data governance, analytics, and compliance initiatives within a life sciences environment.
Key Responsibilities:
Design and implement end-to-end data architecture solutions aligned with business and regulatory requirements.
Work closely with cross-functional teams to ensure data consistency and compliance with IDMP, ISO, and other regulatory frameworks.
Build and optimize data pipelines for ingestion, transformation, and validation of regulatory and clinical data.
Develop data models and metadata repositories to support regulatory submissions and reporting.
Collaborate with business analysts, data engineers, and regulatory teams to translate compliance requirements into data architecture designs.
Ensure adherence to data governance, data quality, and security standards.
Support audits and validation activities by maintaining accurate and compliant data documentation.
Required Skills & Experience:
10+ years of experience in data architecture, data engineering, or related fields.
Hands-on experience with IDMP (Identification of Medicinal Products) or other regulatory data models.
Strong understanding of Regulatory & Compliance frameworks within the pharmaceutical or life sciences domain.
Expertise in data modeling, ETL design, and data integration tools (e.g., Informatica, Talend, Azure Data Factory).
Proficiency in SQL, data warehousing, and cloud data platforms (Azure / AWS preferred).
Experience with data governance and master data management (MDM).
Knowledge of clinical trial data structures and submission processes (a plus).
Excellent communication and stakeholder management skills.
Preferred Skills:
Experience working with IDMP compliance systems and Regulatory Information Management (RIM) tools.
Knowledge of Pharma regulatory submissions (xEVMPD, ISO IDMP, EMA).
Familiarity with data privacy and validation practices (GxP, 21 CFR Part 11).
Job Types: Full-time, Contract
Pay: $101,654.56 - $130,000.00 per year
Work Location: In person
Job Overview:
We are looking for a highly skilled Data Architect with strong experience in Regulatory, Compliance, and IDMP (Identification of Medicinal Products) domains. The ideal candidate will design and manage enterprise data models, regulatory data pipelines, and integration frameworks supporting data governance, analytics, and compliance initiatives within a life sciences environment.
Key Responsibilities:
Design and implement end-to-end data architecture solutions aligned with business and regulatory requirements.
Work closely with cross-functional teams to ensure data consistency and compliance with IDMP, ISO, and other regulatory frameworks.
Build and optimize data pipelines for ingestion, transformation, and validation of regulatory and clinical data.
Develop data models and metadata repositories to support regulatory submissions and reporting.
Collaborate with business analysts, data engineers, and regulatory teams to translate compliance requirements into data architecture designs.
Ensure adherence to data governance, data quality, and security standards.
Support audits and validation activities by maintaining accurate and compliant data documentation.
Required Skills & Experience:
10+ years of experience in data architecture, data engineering, or related fields.
Hands-on experience with IDMP (Identification of Medicinal Products) or other regulatory data models.
Strong understanding of Regulatory & Compliance frameworks within the pharmaceutical or life sciences domain.
Expertise in data modeling, ETL design, and data integration tools (e.g., Informatica, Talend, Azure Data Factory).
Proficiency in SQL, data warehousing, and cloud data platforms (Azure / AWS preferred).
Experience with data governance and master data management (MDM).
Knowledge of clinical trial data structures and submission processes (a plus).
Excellent communication and stakeholder management skills.
Preferred Skills:
Experience working with IDMP compliance systems and Regulatory Information Management (RIM) tools.
Knowledge of Pharma regulatory submissions (xEVMPD, ISO IDMP, EMA).
Familiarity with data privacy and validation practices (GxP, 21 CFR Part 11).
Job Types: Full-time, Contract
Pay: $101,654.56 - $130,000.00 per year
Work Location: In person
