Remote EDC Trial Designer (Clinical Data Capture)

IQVIA Argentina; Durham (NC); On-site; USD 69,000 - 171,000; Full time

Job summary

IQVIA is seeking an EDC Clinical Trial Designer for a remote role based in the United States. The position focuses on designing eCRF forms using Central Designer/Studio or Veeva CDMS/Studio and ensuring regulatory guidelines are followed to deliver high-quality data collection tools for clinical trials.

The role requires a BA/BS and at least 2 years of clinical data management experience with electronic data capture systems, plus strong communication, attention to detail, and multitasking

Qualifications

• BA/BS degree; commensurate experience considered.
• Minimum of 2 years of Clinical Data Management experience using electronic data capture systems.
• Effective oral and written presentation and communication skills.
• Strong attention to detail and a commitment to high quality work with minimal errors.
• Ability to manage multiple project tasks in a fast-paced, evolving environment.
• Experience in planning and management of clinical trials in biopharma or related field preferred.
• Familiarity with CDISC/CDASH/SDTM standards preferred.

Responsibilities

• Proficiency with Central Designer/Studio: understand data collection requirements and study team inputs.
• Work with libraries and create new forms when suitable forms do not exist.
• Produce annotated study books.
• Understand workflow design, dynamic forms and events.
• Validate study design for forms and schedule design; test steps and QC of forms.
• Assist with data integrations, local lab management and coding functionality.
• Input into post-production form changes for live trials.
• Apply lessons learned from one study build to the next.
• Lead meetings with study team to communicate scope, timelines, and requirements.
• Maintain knowledge of regulatory requirements, industry trends and best practices in data management and database design.

Skills

Oral and written communication

Attention to detail

Multi-tasking

Project management

Clinical Data Management

CDISC/CDASH/SDTM familiarity

Education

BA/BS degree

Job description

IQVIA is seeking an EDC Clinical Trial Designer for a remote role based in the United States. The position focuses on designing eCRF forms using Central Designer/Studio or Veeva CDMS/Studio and ensuring regulatory guidelines are followed to deliver high-quality data collection tools for clinical trials.

The role requires a BA/BS and at least 2 years of clinical data management experience with electronic data capture systems, plus strong communication, attention to detail, and multitasking