Clinical Data Standards Lead - Medidata RAVE

IQVIA; Austin (TX); On-site; USD 85,000 - 212,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Data Standards professional to drive Medidata RAVE and global library development across study teams worldwide. The role emphasizes CDISC standards, SDTM mappings, and collaboration with CROs and data managers to ensure compliant data collection and efficient study execution.

The position requires extensive RAVE expertise, strong C# programming skills, and proven governance experience. Join a global team shaping data standards for clinical trials.

Qualifications

• Must have Medidata RAVE experience.
• Must have Medidata RAVE Custom Functions experience.
• Must have C# programming experience.
• Must have Standards Governance experience (CDISC).

Responsibilities

• Develop and maintain global clinical data standards and SDTM mappings.
• Manage Medidata Rave global library objects and CRF completion guidelines.
• Lead standards governance and committee support activities.
• Ensure compliance with CDISC guidelines and regulatory requirements.
• Collaborate with study teams and external partners.

Skills

Medidata RAVE

RAVE Custom Functions

C# programming

Standards Governance

Education

MS/MA in Life Sciences

BS/BA in Life Sciences

High School degree

Tools

CRF Design Tools

Job description

IQVIA is seeking a Senior Clinical Data Standards professional to drive Medidata RAVE and global library development across study teams worldwide. The role emphasizes CDISC standards, SDTM mappings, and collaboration with CROs and data managers to ensure compliant data collection and efficient study execution.

The position requires extensive RAVE expertise, strong C# programming skills, and proven governance experience. Join a global team shaping data standards for clinical trials.