Study Start Up Associate I (regulatory - Office With Flex)

ICON Broadbean

Buenos Aires, Argentina
Hybrid
Proficient knowledge of ich/gcp
Experience with regulatory submissions
Strong attention to detail
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • As a Site Specialist I, you will support investigator sites with key administrative and operational activities.
  • ICON offers a range of additional benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • Proficient knowledge of ICH/GCP
  • Experience with regulatory submissions
  • Strong attention to detail

Nice-to-have

  • Ability to work independently
  • Excellent communication skills
  • Fast-paced environment adaptability

Key Requirements

  • Bachelor’s Degree in Life Sciences
  • 2 years’ experience in clinical study start up
  • Knowledge of regulatory processes

Work Rights

Not specified

Tailored Resume

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