Specialist, Site Contracts - Japan- Remote

Worldwide Clinical Trials

Japan
1-3 years clinical research experience
Site contract negotiation proficiency
Ich-gcp and regulatory knowledge
The role involves reviewing, analyzing, and drafting clinical research site contracts while negotiating terms and budgets with sites globally

Job Summary

  • The role involves reviewing, analyzing, and drafting clinical research site contracts while negotiating terms and budgets with sites globally.
  • Candidates must possess a strong understanding of international and local regulatory requirements including FDA, EMA, and ICH-GCP guidelines.
  • The company fosters a diverse and inclusive environment where professionals are encouraged to take pioneering approaches to improve patient lives.

Matching Summary

The role involves reviewing, analyzing, and drafting clinical research site contracts while negotiating terms and budgets with sites globally.

Skills & Requirements

Must-have

  • 1-3 years clinical research experience
  • Site contract negotiation proficiency
  • ICH-GCP and regulatory knowledge
  • MS Office suite proficiency
  • English language fluency

Nice-to-have

  • Strong problem-solving skills
  • Ability to work under pressure
  • High level of accuracy in drafting
  • Experience with contract management software

Key Requirements

  • Bachelor's Degree in business, finance, or science
  • 1 to 3 years experience in CRO or pharmaceutical industry
  • Proficiency in MS Word, Excel, and Outlook

Work Rights

Not specified

Tailored Resume

Cover Letter