USDM Programmer

Overview

Remote
$120 - $125
Contract - W2
Contract - 06 Month(s)

Skills

USDM Programmer

Job Details

Immediate need for a talented USDM Programmer. This is a 06+ months contract opportunity with long-term potential and is located in US(Remote). Please review the job description below and contact me ASAP if you are interested.

Job ID: 25-84967

Pay Range: $120 - $125/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

  • Protocol Ingestion & Transformation
  • Support the transformation of protocol data into USDM-compliant representations that can be consumed by pharma sponsors.
  • Ensure accurate mapping across CTMS, FHIR (client and industry), and sponsor systems.
  • Sponsor-Ready Deliverables
  • Validate completeness and accuracy of USDM outputs against protocol source documents.
    Package and deliver USDM representations in formats directly usable by pharma companies.
  • Act as a subject matter expert in explaining how sponsor protocols map into USDM.
  • Data Model Mapping
  • Lead efforts to map internal CTMS models FHIR USDM, ensuring interoperability.
  • Build robust pipelines that maintain traceability from PDF protocol FHIR USDM.
  • Define standards, templates, and validation checks to ensure consistency across studies.
  • Standards & Process Leadership
  • Serve as the internal authority on USDM concepts (elements, metadata, best practices, processes).
  • Guide prioritization of protocol concepts most critical to sponsors and regulators.
  • Collaborate with Product, Engineering, and other cross-functional stakeholders to align protocol digitization workflows with regulatory and industry standards.

Key Requirements and Technology Experience:

  • 5 7 years of experience in clinical data standards, data management, or programming within pharma/biotech/clinical research.
  • 2 3 years of hands-on experience with USDM / *** MUST BE EXPERT LEVEL ***
  • Hands-on experience with CTMS systems and FHIR standards, including data model mapping.
  • Practical experience in document parsing, text mining, or NLP/AI for unstructured data ingestion.
  • Strong communication skills, with ability to interface directly with pharma sponsors and explain technical mappings
  • Experience validating structured outputs against sponsor and regulatory requirements.
  • Knowledge of clinical data interoperability frameworks and submission standards.
  • Strong Expertise in CDISC standards (SDTM, ADaM) and regulatory expectations for protocol data.
  • Experience with protocol digitization initiatives in pharma/biotech/clinical research.
  • Strong programming background (Python, SQL, or equivalent) with experience in ETL pipelines and data transformations.

Our client is a leading Health care Biotechnology Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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