Regulatory And Start Up Specialist - Israel

IQVIA UK

Multiple Locations
Experience with submissions in israel
Fluency in hebrew
Knowledge of gcp/ich guidelines
This role involves performing tasks associated with Site Activation activities according to applicable regulations and SOPs

Job Summary

  • This role involves performing tasks associated with Site Activation activities according to applicable regulations and SOPs.
  • The position requires ensuring adherence to project timelines and quality of deliverables.
  • Local expertise is provided to project teams during planning and execution of studies.

Matching Summary

This role involves performing tasks associated with Site Activation activities according to applicable regulations and SOPs.

Skills & Requirements

Must-have

  • Experience with submissions in Israel
  • Fluency in Hebrew
  • Knowledge of GCP/ICH guidelines

Nice-to-have

  • Ability to apply regulatory requirements
  • Experience in leadership capacity
  • Understanding of drug development process

Key Requirements

  • Bachelor’s Degree in life sciences
  • 3 years clinical research experience
  • 1 year experience in leadership capacity

Work Rights

Not specified

Tailored Resume

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