EDC Trial Design Specialist

ICON Strategic Solutions; United Kingdom; On-site; GBP 45,000 - 70,000; Full time

Job summary

ICON plc is seeking a Clinical System Designer II to create high quality data collection tools for clinical trials and manage eCRF design using Oracle InForm/Central Designer or Veeva CDMS/Studio. You will work with study teams to ensure quality, timelines and regulatory compliance.

Required: BA/BS and 2+ years in clinical data management with eCRF systems; strong communication, attention to detail and ability to handle multiple tasks in a dynamic environment.

Qualifications

• BA/BS degree or commensurate experience.
• Minimum 2 years of Clinical Data Management with electronic data capture systems.
• Strong written and verbal communication skills.
• Ability to manage multiple tasks in a fast-paced environment.
• Familiarity with CDISC/CDASH/SDTM standards preferred.

Responsibilities

• Design and develop high quality data collection tools for clinical trials using eCRF design.
• Create and annotate study books; validate study design and formats.
• Collaborate with study team to communicate work scope and timelines.
• Support post-production form changes and regulatory compliance awareness.

Skills

Communication skills

Attention to detail

Presentation skills

Multitasking

Education

BA/BS degree

Tools

Oracle InForm/Central Designer

Veeva CDMS/Studio

Job description

ICON plc is seeking a Clinical System Designer II to create high quality data collection tools for clinical trials and manage eCRF design using Oracle InForm/Central Designer or Veeva CDMS/Studio. You will work with study teams to ensure quality, timelines and regulatory compliance.

Required: BA/BS and 2+ years in clinical data management with eCRF systems; strong communication, attention to detail and ability to handle multiple tasks in a dynamic environment.