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Systems Designer​/Analyst II

Job in Newark, Essex County, New Jersey, 07175, USA
Listing for: The Fountain Group LLC
Full Time position
Listed on 2026-07-25
Job specializations:
  • IT/Tech
    Information Security & Data Protection
Salary/Wage Range or Industry Benchmark: 42 - 46 USD Hourly USD 42.00 46.00 HOUR
Job Description & How to Apply Below
Position: Systems Designer / Analyst II

The Fountain Group is currently seeking a Systems Designer / Analyst II for a prominent client of ours. This position is located in Branchburg, NJ . Details for the position are as follows:

Job Title: Clinical Data Systems Lead (EDC Study Build)
Location: Prefer New Jersey or near a client office (Open to remote candidates with strong experience)
Pay Rate: $42-$46/hr (W2)
Duration: 1 Year (Potential extension for a 2nd year)

Job Description
  • Lead the design, build, and delivery of clinical trial systems, including EDC, IRT, and ePRO.
  • Develop and implement common data standards across clinical studies.
  • Perform hands-on technical study build in Medidata Rave while ensuring compliance with protocol and data standards.
  • Ensure consistency of clinical system design across therapeutic areas and programs.
  • Manage system integrations and coordinate required study updates.
  • Track study build progress and ensure timely delivery using project management methodologies.
  • Ensure compliance with GCP, ICH Guidelines, SOPs, and applicable regulatory requirements.
  • Lead process improvement and innovation initiatives within Clinical Data Strategy.
Education
  • Bachelor's degree in Business, Management Information Systems, Computer Science, Life Sciences, or a related field.
  • Master's degree preferred.
Required Skills
  • 7+ years of hands-on technical study build experience in Medidata Rave EDC
  • Clinical Electronic Data Capture (EDC) system design and configuration
  • CDASH standards
  • SDTM standards
  • Clinical trial system implementation (EDC, IRT, ePRO)
  • Clinical data standards development
  • Clinical trial process expertise
  • GCP, ICH Guidelines, and clinical regulatory compliance
Preferred Skills
  • Veeva EDC technical study build experience
  • Clinical system integration experience
  • Clinical Data Strategy process improvement and standardization
  • Cross-study/program clinical system design expertise
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