Clinical Data Systems Designer (Medidata RAVE)

The Fountain Group is a national staffing firm and we are currently seeking a ­­­­­­­­Clinical Data Systems Designer (Medidata RAVE) for a prominent client of ours. This position is REMOTE or Local to Branchburg, NJ (Preferred) Details for the position are as follows:

• Clinical Data Systems Designer (Medidata RAVE)
• Pay: $42–46/hour
• Duration: 1-year contract with strong potential for extension
• Location: Prefer candidates based in New Jersey but open to remote candidates with the required experience.

• We're seeking an experienced Clinical Data Systems Designer to support the design and implementation of electronic data capture (EDC) systems for global clinical trials. This role partners closely with Clinical Data Management, Clinical Operations, and cross-functional teams to develop high-quality clinical systems that support data collection, regulatory compliance, and study execution.
• The ideal candidate has extensive Medidata RAVE study build experience and a strong understanding of clinical trial data standards, including CDASH.

Responsibilities

• Design, build, and maintain clinical trial databases in Medidata RAVE EDC
• Develop electronic Case Report Forms (eCRFs) and system functionality aligned with protocol requirements and CDASH standards
• Ensure consistency across studies and therapeutic area programs by applying standardized design methodologies
• Support implementation and integration of clinical systems, including EDC, IRT, ePRO, and related technologies
• Manage study build timelines, system updates, amendments, and deliverables across multiple clinical programs
• Identify project risks and proactively develop solutions to maintain quality and timelines
• Collaborate with Clinical Data Management, Clinical Operations, Biostatistics, Programming, and external vendors throughout study execution
• Ensure compliance with GCP, ICH guidelines, regulatory requirements, and internal SOPs
• Mentor junior team members and contribute to continuous improvement initiatives within Clinical Data Systems

Qualifications

• Bachelor's degree in Life Sciences, Computer Science, Information Systems, or a related discipline
• 4+ years of hands-on Medidata RAVE EDC study build experience
• Demonstrated experience designing and configuring clinical trial databases
• Strong understanding of CDASH standards and clinical data collection principles
• Working knowledge of SDTM and downstream clinical data processes
• Experience supporting complex global clinical studies within pharmaceutical, biotechnology, or CRO environments
• Veeva EDC experience is a plus
• Excellent communication, organization, and project management skills with the ability to work across cross-functional teams

• Preferred Experience
• Global clinical trial experience
• Experience with multiple clinical systems integrations (EDC, IRT, ePRO)
• Process improvement and standardization initiatives
• Technical leadership or mentoring experience

• Why You'll Love This Opportunity
• Join a highly collaborative Clinical Data Strategy organization supporting innovative clinical development programs.
• Work with modern clinical technologies while helping shape data standards and study design across multiple global clinical trials.
• Long-term contract with strong extension potential and exposure to high-impact clinical development initiatives.