

The Fountain Group
Systems Designer / Analyst II
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Systems Designer / Analyst II in Branchburg, NJ, with a 1-year contract at $42-$46/hr. Requires 7+ years in Medidata Rave EDC, clinical data standards, and compliance knowledge. Remote candidates with strong experience are considered.
🌎 - Country
United States
💱 - Currency
$ USD
-
💰 - Day rate
368
-
🗓️ - Date
July 24, 2026
🕒 - Duration
More than 6 months
-
🏝️ - Location
Hybrid
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📄 - Contract
W2 Contractor
-
🔒 - Security
Unknown
-
📍 - Location detailed
Branchburg, NJ
-
🧠 - Skills detailed
#MIS Systems (Management Information Systems) #Medidata Rave #Strategy #Project Management #GCP (Google Cloud Platform) #Compliance #AI (Artificial Intelligence) #Data Strategy #Computer Science
Role description
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
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy
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
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy






