Regulatory Maintenance Associate (clinical Trials)

IQVIA UK

**
Bachelor's degree in lifescience
1-2 years eu ctis experience
Global core pack knowledge
** IQVIA UK is seeking a Regulatory Maintenance Associate to support clinical trial submissions through the preparation and review of regulatory documents. The ideal candidate should have a Life Science degree, relevant experience, and strong communication skills to manage projects and interact with clients effectively. **

Job Summary

  • The role involves preparing and reviewing regulatory documents to support clinical trial submissions in accordance with applicable requirements.
  • Candidates will act as a Clinical Trial Regulatory Manager on straightforward projects while receiving guidance on complex regulatory initiatives.
  • The position requires maintaining core clinical trial submission dossiers and ensuring high-quality deliverables across internal systems and databases.

Matching Summary

Match Score: 75

** IQVIA UK is seeking a Regulatory Maintenance Associate to support clinical trial submissions through the preparation and review of regulatory documents. The ideal candidate should have a Life Science degree, relevant experience, and strong communication skills to manage projects and interact with clients effectively. **

Skills & Requirements

Must-have

  • Bachelor's Degree in Lifescience
  • 1-2 years EU CTIS experience
  • Global core pack knowledge
  • Country oversight for amendments
  • R&D process understanding

Nice-to-have

  • Strategic planning for submissions
  • Independent thought for improvements
  • Effective client relationships
  • Self-motivation and enthusiasm
  • Process improvement assistance

Key Requirements

  • Bachelor's Degree in Lifescience or related discipline
  • 1-2 years relevant experience with EU CTIS
  • Experience in country oversight particularly for amendments

Work Rights

Not specified

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