Senior Clinical Data Designer - eCRF/RAVE Expert

IQVIA LLC; Durham (NC); On-site; USD 69,000 - 171,000; Full time

Job summary

IQVIA is seeking a RAVE designer to lead study build and design, edit specifications, and configure systems for clinical trials. You will collaborate with DTL, programmers, validation teams, vendors, statisticians, and client representatives to ensure accurate study design and timely delivery.

Responsibilities include designing the eCRF in Medidata RAVE and other platforms, creating edit specs, reviewing budgets, and monitoring timelines and risks across multiple studies.

Qualifications

• Bachelor's degree in science/IT or related field.
• 2–4 years of RAVE designer experience; total experience 7+ years.

Responsibilities

• Interpret the study protocol and design the eCRF in Medidata RAVE and other platforms.
• Create and update Edit Specification documents.
• Generate specifications for EDC build components (Rights and Roles, System Settings, Home Page).
• Review timelines and budgets; manage risks and budgets for own projects.
• Collaborate with Data Team Lead, programmers, validation team, vendors, statisticians, and clients.

Education

Bachelor's Degree in Science/Computer science/Information Technology or Bachelor in Technology

Tools

Medidata RAVE

Job description

IQVIA is seeking a RAVE designer to lead study build and design, edit specifications, and configure systems for clinical trials. You will collaborate with DTL, programmers, validation teams, vendors, statisticians, and client representatives to ensure accurate study design and timely delivery.

Responsibilities include designing the eCRF in Medidata RAVE and other platforms, creating edit specs, reviewing budgets, and monitoring timelines and risks across multiple studies.