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Senior Medical device documentation Associate

Remote, USA Full-time Posted 2026-06-25

When our values align, there's no limit to what we can achieve.   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Medical device documentation- Diagnostic Imaging and Interventional Radiology

  • Knowledge of contrast media, injectors and disposables in medical imaging (MRI/CT)
  • Experience in dossier preparation, compilation and submission for medical devices based on the legal manufacturer/physical manufacturer elements and the technical documentation
  • Good understanding- of the medical imaging devices compliance from a global and regional perspective, registration procedures, preparation of answers to questions from health authorities
  • Identification of regulatory risks and impact 
  • Experience in identifying label specific requirements and appropriate process and/or relabeling
  • Expertise with regulatory management system and document management systems
  • Effective communication and collaboration skills, and the ability to work independently
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