job summary: Join a top-tier global pharmaceutical leader as a Systems Designer / Analyst II, driving innovation in clinical trial data systems. This role offers flexible location options, with a preference for Branchburg, NJ, proximity to a company office, or full remote flexibility for candidates with strong Medidata Rave expertise.

location: Somerville, New Jersey job type: Contract salary: $50.00 - 60.92 per hour work hours: 9 to 5 education: Bachelors

responsibilities:

• Conduct hands-on design of clinical studies and author detailed EDC specifications from scratch.
• Develop common data standards and build EDC systems ensuring strict compliance with protocols, GCP, and ICH guidelines.
• Lead cross-functional collaboration across study teams, monitoring groups, clinical scientists, and statistical teams.
• Ensure on-time delivery of clinical systems (EDC, IRT, ePRO), system integrations, and protocol changes.
• Establish system design methodologies that optimize functionality, end-user experience, and clinical data flow.
• Actively participate in study reviews, navigate team dynamics, and close out clinical trials smoothly.

qualifications: Required:

• Bachelor’s degree with 6-7+ years of experience, or Master’s/Ph.D. with 3-4+ years of relevant experience.
• 7+ years of hands-on technical study build experience in Medidata Rave (Day 1 requirement).
• Proven experience building EDC specifications from scratch and hands-on CDASH/SDTM knowledge.
• Strong cross-functional coordination, project management, and collaboration skills.
• Willingness to work hybrid (3 days onsite / 2 days WFH) upon potential FTE conversion.

Preferred:

• Phase I experience (specifically Aesthetic/Eyecare specialties) or broad therapeutic background (Oncology, Neurology, Immunology).
• Prior experience with Veeva EDC technology.

LI-MH1

skills: EDC (Electronic Data Capture), Medidata

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

,

• Conduct hands-on design of clinical studies and author detailed EDC specifications from scratch.
• Develop common data standards and build EDC systems ensuring strict compliance with protocols, GCP, and ICH guidelines.
• Lead cross-functional collaboration across study teams, monitoring groups, clinical scientists, and statistical teams.
• Ensure on-time delivery of clinical systems (EDC, IRT, ePRO), system integrations, and protocol changes.
• Establish system design methodologies that optimize functionality, end-user experience, and clinical data flow.
• Actively participate in study reviews, navigate team dynamics, and close out clinical trials smoothly.

EDC (Electronic Data Capture), Medidata