Senior Clinical Data Designer: eCRF & EDC Expert

IQVIA LLC; England; Sur place; GBP 42 000 - 62 000; Plein temps

Résumé du poste

IQVIA is seeking a Technical Designer to lead study build and design activities, and manage updates to specifications and eCRF configurations. You will work with DTL, programmers, validation teams, vendors, statisticians, and client representatives to ensure timely, accurate study delivery.

The role involves developing CDMS specifications aligned with SDTM/CDASH standards, creating Edit Specifications, and contributing to risk management and process improvements across multiple projects.

Qualifications

• Bachelor's degree required in science/computer science/IT or technology field.
• 2–4 years of core Technical Designer experience; total experience 7+ years.
• Experience collaborating with DTL, Programmer, Validation Team, vendors, statisticians, and client representatives.

Responsabilités

• Interpret the study protocol.
• Design and update the eCRF using CDMS tools in line with SDTM/CDASH standards.
• Create and update Edit Specification Document and generate specifications for EDC components.
• Support Study Authorization and Trial Capacity processes; attend and lead reviews.
• Identify project risks and communicate them to the Data Team Lead; escalate quality issues.

Connaissances

Technical design

Client communication

Formation

Bachelor's degree in Science/CS/IT or B.Tech

Description du poste

IQVIA is seeking a Technical Designer to lead study build and design activities, and manage updates to specifications and eCRF configurations. You will work with DTL, programmers, validation teams, vendors, statisticians, and client representatives to ensure timely, accurate study delivery.

The role involves developing CDMS specifications aligned with SDTM/CDASH standards, creating Edit Specifications, and contributing to risk management and process improvements across multiple projects.