Clinical Research Associate

Bristor Myers Squibb

Otemachi, Japan
50% onsite
Monitoring clinical trial progress
Ensure compliance with gcp
Site relationship management
Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s)

Job Summary

  • Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s).
  • Act as one of the points of contact at a Site level for internal and external stakeholders.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.

Matching Summary

Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s).

Skills & Requirements

Must-have

  • monitoring clinical trial progress
  • ensure compliance with GCP
  • site relationship management
  • data integrity and quality assurance
  • risk assessment and issue resolution

Nice-to-have

  • proactive problem identification
  • mentoring and coaching colleagues
  • adaptability and flexibility
  • strong stakeholder communication

Key Requirements

  • Bachelors degree in life sciences or equivalent
  • 1+ year relevant clinical research experience (Associate CRA)
  • 2-3 years relevant clinical research experience (CRA)
  • 5+ years monitoring experience (Senior CRA)
  • Knowledge of ICH/GCP Guidelines and local regulations

Work Rights

Not specified

Tailored Resume

Cover Letter