Remote EDC Clinical Trial Designer: Data & Form Expert

PPG US ProPharma Group, LLC; Raleigh (NC); Hybrid; USD 85,000 - 120,000; Full time

Job summary

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

The role requires experience with Oracle InForm/Central Designer or Veeva CDMS/Studio, plus familiarity with CDISC/CDASH/SDTM standards to ensure timely, compliant deliverables.

Qualifications

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

Responsibilities

• Design and develop data collection tools for new clinical trials.
• Design of eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio.
• Validate study design for forms and schedule.
• Test steps development and QC of forms.
• Coordinate with study team on timelines and requirements.
• Maintain regulatory knowledge and industry best practices in data management.

Skills

Communication skills

Attention to detail

Time management

Team collaboration

Education

BA/BS degree

Tools

Oracle InForm/Central Designer

Veeva CDMS/Studio

Job description

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

The role requires experience with Oracle InForm/Central Designer or Veeva CDMS/Studio, plus familiarity with CDISC/CDASH/SDTM standards to ensure timely, compliant deliverables.