EDC Trial Designer: Build precise eCRF forms

IQVIA Argentina; Reading; On-site; GBP 45,000 - 65,000; Full time

Job summary

IQVIA in Reading, United Kingdom, is seeking an EDC Clinical Trial Designer to build high-quality data collection tools for new trials and support design, development, testing and implementation of clinical eCRF databases.

Designs eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio and ensures SOPs, CRF standards and trial guidelines are implemented to meet timelines and deliverables with quality data.

Qualifications

• 2+ years of Clinical Data Management using electronic data capture systems.
• Familiarity with CDISC/CDASH/SDTM standards.
• Effective oral and written communication skills.
• Attention to detail with high quality work and low error rate.
• Experience planning and managing clinical trials in biopharma or related field.

Responsibilities

• Create high quality data collection tools for new clinical trials.
• Design and implement eCRF databases; develop and test forms.
• Ensure SOPs, CRF standards, and guidelines are applied.
• Collaborate with study team on workflow design and form events.
• Conduct meetings to communicate scope, timelines and requirements.
• Maintain knowledge of regulatory trends and data management best practices.

Skills

eCRF design

Oracle InForm

Veeva CDMS

Clinical Data Management

Regulatory awareness

Education

BA/BS degree

Tools

Central Designer/Studio

Veeva CDMS/Studio

Job description

IQVIA in Reading, United Kingdom, is seeking an EDC Clinical Trial Designer to build high-quality data collection tools for new trials and support design, development, testing and implementation of clinical eCRF databases.

Designs eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio and ensures SOPs, CRF standards and trial guidelines are implemented to meet timelines and deliverables with quality data.