Site Activation Specialist - Japan - Remote

Worldwide Clinical Trials

Japan
Track study-specific site regulatory documents
Review country/site specific informed consent forms
Maintain regular communication with clinical sites
The role involves facilitating the efficient activation of clinical research sites as an integral part of the Site team

Job Summary

  • The role involves facilitating the efficient activation of clinical research sites as an integral part of the Site team.
  • Candidates will support the development and review of country-specific informed consent forms while maintaining regular communication with sites.
  • Worldwide Clinical Trials prioritizes cultivating a diverse and inclusive environment where professionals thrive by being themselves.

Matching Summary

The role involves facilitating the efficient activation of clinical research sites as an integral part of the Site team.

Skills & Requirements

Must-have

  • Track study-specific site regulatory documents
  • Review country/site specific informed consent forms
  • Maintain regular communication with clinical sites
  • Collect and review required study-specific documents
  • Support Site Identification activities

Nice-to-have

  • Strong organizational and time management skills
  • Ability to handle multiple tasks in fast-paced environment
  • Proficiency in MS-Office applications
  • Understanding of local healthcare systems
  • Multilingualism preferred

Key Requirements

  • Minimum four-year college degree in science or related field
  • One year of experience in clinical research
  • Previous experience within pharmaceutical or CRO industry
  • Good knowledge of ICH GCP and EU Clinical Trials Directive
  • Fluent in local language with working knowledge of English

Work Rights

Not specified

Tailored Resume

Cover Letter