EDC Trial Designer — Data Capture & eCRF Expert

IQVIA; North Carolina; On-site; USD 69,000 - 171,000; Full time

Job summary

IQVIA seeks an EDC Clinical Trial Designer to create high quality data collection tools for new trials and support design, testing and implementation of clinical eCRF databases.

Responsibilities include designing forms with Central Designer/Studio or Veeva CDMS/Studio, ensuring SOPs and trial guidelines are followed, and coordinating with study teams to meet timelines. Requires 2+ years in Clinical Data Management and familiarity with CDISC standards.

Qualifications

• Minimum 2 years of Clinical Data Management experience using electronic data capture systems.
• Experience with eCRF design and data collection tools.
• Familiarity with regulatory requirements and industry standards.

Responsibilities

• Design eCRF forms using Central Designer/Studio or Veeva CDMS/Studio.
• Validate study design and form/schedule workflows.
• Create annotated study books and perform QC on forms.
• Communicate scope and timelines to the study team.

Skills

Clinical Data Management

Central Designer/Studio

eCRF design

Regulatory awareness

Education

BA/BS degree

Tools

CDISC/CDASH/SDTM

Job description

IQVIA seeks an EDC Clinical Trial Designer to create high quality data collection tools for new trials and support design, testing and implementation of clinical eCRF databases.

Responsibilities include designing forms with Central Designer/Studio or Veeva CDMS/Studio, ensuring SOPs and trial guidelines are followed, and coordinating with study teams to meet timelines. Requires 2+ years in Clinical Data Management and familiarity with CDISC standards.