R&d Oncology Clinical Science Clinical Research Sr. Scientist

Merck Sharp & Dohme Corp

Tokyo, Japan
Hybrid
3+ years pharmaceutical clinical development experience
Protocol development and creation experience
Strong english communication skills (toeic 730+)
Merck Sharp & Dohme Corp is seeking a Senior Scientist for their Oncology Clinical Science department in Tokyo, Japan. The role involves collaboration on clinical trials and developing strategic plans for drug approvals, requiring strong communication skills and experience in oncology clinical development

Job Summary

  • This role involves contributing to the global simultaneous development of groundbreaking new cancer treatments through close collaboration with various departments.
  • The successful candidate will serve as a key member of the clinical trial team, supporting strategy formulation, regulatory interactions, and approval applications in Japan.
  • The position offers significant professional growth opportunities in scientific expertise, communication skills, and logical thinking within a supportive team environment.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking a Senior Scientist for their Oncology Clinical Science department in Tokyo, Japan. The role involves collaboration on clinical trials and developing strategic plans for drug approvals, requiring strong communication skills and experience in oncology clinical development.

Skills & Requirements

Must-have

  • 3+ years pharmaceutical clinical development experience
  • Protocol development and creation experience
  • Strong English communication skills (TOEIC 730+)
  • Collaboration with internal and external medical experts
  • Knowledge of ICH GCP guidelines

Nice-to-have

  • Oncology specific clinical trial experience
  • Experience with global trial negotiations
  • Medical writing and publication support skills
  • Strategic planning for early and late stage trials

Key Requirements

  • Minimum 3 years of pharmaceutical clinical development experience
  • Proven experience in creating Investigational New Drug protocols
  • English proficiency equivalent to TOEIC score of 730 or higher
  • Experience with PMDA regulatory submissions and inquiries

Work Rights

Not specified

Sponsorship: available

Tailored Resume

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