Study Start Up Manager (ssum)

IQVIA Inc

Hybrid
Strong local israeli regulatory knowledge
Fluency in arabic language required
Experience with pre-award bid defense activities
The role involves directing and managing the delivery of all required site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs

Job Summary

  • The role involves directing and managing the delivery of all required site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs.
  • Candidates must possess strong local experience and knowledge in Israeli regulations and submissions along with fluency in Arabic.
  • The position requires a thorough understanding of the regulated clinical trial environment and the ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Matching Summary

The role involves directing and managing the delivery of all required site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs.

Skills & Requirements

Must-have

  • Strong local Israeli regulatory knowledge
  • Fluency in Arabic language required
  • Experience with pre-award bid defense activities
  • Knowledge of GCP and ICH guidelines
  • Oversight of multi-regional study programs

Nice-to-have

  • Ability to mentor and coach colleagues
  • Experience developing client relationships
  • Skill in delivering presentations to clients
  • Creative problem solving for regulatory challenges

Key Requirements

  • Bachelor's Degree in Life Sciences or related field
  • 7 years' relevant experience in scientific or clinical environment
  • Demonstrable experience in an international role

Work Rights

Must have strong local experience and knowledge in Israeli regulations

Tailored Resume

Cover Letter