Site Activation Partner - Fsp

Parexel

Seoul, South Korea
Clinical trial management
Regulatory document submission
Site activation coordination
At Parexel, we share the goal of improving the world's health through clinical development solutions. The role involves coordinating site activation activities and ensuring compliance with regulatory requirements. You will contribute to the development of therapies that ultimately benefit patients, working with empathy and commitment

Job Summary

  • At Parexel, we share the goal of improving the world's health through clinical development solutions. The role involves coordinating site activation activities and ensuring compliance with regulatory requirements. You will contribute to the development of therapies that ultimately benefit patients, working with empathy and commitment.

Matching Summary

At Parexel, we share the goal of improving the world's health through clinical development solutions. The role involves coordinating site activation activities and ensuring compliance with regulatory requirements. You will contribute to the development of therapies that ultimately benefit patients, working with empathy and commitment.

Skills & Requirements

Must-have

  • Clinical trial management
  • Regulatory document submission
  • Site activation coordination

Nice-to-have

  • Effective communication skills
  • Ability to work independently
  • Attention to detail

Key Requirements

  • Minimum 2 years' relevant experience
  • Fluency in local language and English
  • Education in life sciences preferred

Work Rights

Not specified

Tailored Resume

Cover Letter