Healthcare Regulatory Specialist

6 hours ago


Reading, Reading, United Kingdom IQVIA, Inc. Full time
About the Role

This is an exciting opportunity for a Healthcare Regulatory Specialist to join our team at IQVIA, Inc. As a key member of our clinical trial support team, you will play a crucial role in ensuring the successful execution of complex projects and programs.

Key Responsibilities
  1. Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer.
  2. Provides administrative and technical/scientific support for core scientific documentation and feedback gap analysis to customers.
  3. Develops and writes scientific documents, such as Investigational Medicinal Product Dossiers, and clinical trial justifications.
Requirements
  • Comprehensive knowledge of regulations, directives, and guidance supporting clinical Research and Development.
  • Excellent communication and negotiation skills.
  • Ability to work independently and as part of a team.
Compensation and Benefits

Estimated salary: $90,000 - $115,000 per year. Benefits include health insurance, 401(k) plan, paid time off, and professional development opportunities.


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