EDC Data Architect for Global Trials

IQVIA

Reading

On-site

GBP 60,000 - 90,000

Full time

27 hours ago
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Job summary

IQVIA in Reading, United Kingdom is seeking an EDC Data Acquisition Expert to define and implement Clinical Electronic Data Capture tools in line with trial protocols. You will collaborate with Data Managers, SRP, SRS, and Biostatisticians to deliver robust data capture solutions.

Responsibilities include designing eCRF layouts, programming edit checks, configuring technical specifications for tSDV and Datamart mappings, performing Rave migrations, and guiding junior staff through build and

Qualifications

  • 5+ years’ experience building EDC databases in clinical research.
  • Technical EDC build experience in Medidata Rave with complex database builds.
  • Demonstrated project management skills.
  • Advanced custom functions programming knowledge.
  • Experience working on clinical trials.
  • Experience working in diverse, cross-functional global teams.
  • Working knowledge of GCP/ICH guidelines and CDASH.

Responsibilities

  • Assess protocol-based EDC collection requirements and create startup eCRF packages.
  • Design eCRF layouts and form dynamics.
  • Program edit checks and custom functions.
  • Create and configure technical specs for tSDV, Safety Gateway, and Datamart mappings.
  • Implement EDC coding configurations per trial coding requirements.
  • Perform test and production Rave EDC migrations.
  • Oversee IWRS integration planning with EDC.
  • Provide SME support for complex EDC database builds and integrations.
  • Train junior staff on EDC build and migration processes.
  • Participate in process and tool improvement initiatives in clinical data management.

Skills

EDC databases
Medidata Rave
Project management
Custom functions programming
Cross-functional teamwork
GCP/ICH knowledge
CDASH knowledge

Tools

Rave EDC

Job description

IQVIA in Reading, United Kingdom is seeking an EDC Data Acquisition Expert to define and implement Clinical Electronic Data Capture tools in line with trial protocols. You will collaborate with Data Managers, SRP, SRS, and Biostatisticians to deliver robust data capture solutions.

Responsibilities include designing eCRF layouts, programming edit checks, configuring technical specifications for tSDV and Datamart mappings, performing Rave migrations, and guiding junior staff through build and

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