EDC Clinical Trial Designer - eCRF Form Architect

IQVIA Argentina; Greater London; Hybrid; GBP 55,000 - 70,000; Full time

Job summary

IQVIA in London is seeking an EDC Clinical Trial Designer to create high quality data collection tools for new trials and support design, development, documentation, testing and implementation of clinical eCRF databases.

Responsibilities include form design using Central Designer/Studio or Veeva CDMS, ensuring SOPs and CDISC standards are followed, and coordinating with the study team to meet timelines and deliverables.

Qualifications

• Minimum of 2 years of Clinical Data Management experience using electronic data capture systems.
• Familiarity with clinical research processes and CDISC/CDASH/SDTM standards.
• Effective oral and written presentation and communication skills.
• Ability to manage multiple project tasks in a fast-paced environment.

Responsibilities

• Design and develop data collection tools for clinical trials.
• Proficiency with Central Designer/Studio and form design.
• Produce annotated study books and validate study design.
• Input into design of post-production form changes to live trials.
• Conduct meetings with the study team to communicate scope and timelines.
• Maintain regulatory knowledge and adherence to best practices.

Skills

Clinical data management

Electronic data capture

CDISC/CDASH/SDTM

Regulatory awareness

Communication skills

Education

BA/BS degree

Tools

Central Designer/Studio

Veeva CDMS/Studio

Job description

IQVIA in London is seeking an EDC Clinical Trial Designer to create high quality data collection tools for new trials and support design, development, documentation, testing and implementation of clinical eCRF databases.

Responsibilities include form design using Central Designer/Studio or Veeva CDMS, ensuring SOPs and CDISC standards are followed, and coordinating with the study team to meet timelines and deliverables.