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IQVIA

Regulatory Affairs Coordinator

IQVIA

. Draft new informed consent forms for new studies and revise current informed consent forms .

Posted 5/8/2026full-timeIrving • Texas • 🇺🇸 United StatesMid-LevelSenior💰 $46,200 - $96,200 per yearWebsite

About the role

Key responsibilities & impact
  • Draft new informed consent forms for new studies and revise current informed consent forms
  • Submit new studies to the Institutional Review Board (IRB) for approval
  • Work with Research Coordinators to ensure all patient-facing material is available
  • Enter study-specific information in internal FileMaker database
  • Attend Phase I meetings and Site Initiation Visit meetings

Requirements

What you’ll need
  • Bachelor’s degree in administration or science
  • At least three-year experience in Regulatory Affairs in a research setting
  • Proficiency in Microsoft Word and Adobe Acrobat
  • Excellent verbal and written communication skills

Benefits

Comp & perks
  • Health insurance
  • Retirement plans
  • Paid time off
  • Flexible work arrangements
  • Professional development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
informed consent formsRegulatory AffairsFileMaker database
Soft Skills
verbal communicationwritten communication