Senior Site Specialist

ICON

Multiple Locations
Regulatory document preparation and submission
Clinical trial start-up coordination
Regulatory compliance management
As a Senior Study Start Up Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Senior Study Start Up Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is committed to providing an inclusive and accessible environment for all candidates and a workplace free of discrimination and harassment.

Matching Summary

As a Senior Study Start Up Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Regulatory document preparation and submission
  • Clinical trial start-up coordination
  • Regulatory compliance management
  • Project management skills
  • Cross-functional team collaboration

Nice-to-have

  • Process improvement initiatives
  • Inclusive and diverse work culture
  • Strong interpersonal communication

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Minimum 4 years clinical research or regulatory affairs experience
  • Experience in study start-up activities
  • Knowledge of ICH-GCP and local regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter