【astrazeneca】【r&d】senior Clinical Research Associate / Clinical Research Associate(oncology), Development Operations, Late Development Oncology Clinical Operation 2

Trzdev35

Osaka, , Japan
Clinical trial site monitoring
Communication with investigators and vendors
Leadership in clinical operations
The Monitor ensures that clinical trials are conducted properly, protecting human subjects and verifying data accuracy and compliance with protocols and regulations

Job Summary

  • The Monitor ensures that clinical trials are conducted properly, protecting human subjects and verifying data accuracy and compliance with protocols and regulations.
  • Senior CRA leads and mentors other CRAs, manages multiple sites with complex protocols, and contributes to clinical operations improvements and initiatives.
  • The role involves active communication with study leaders, investigators, third-party vendors, and regulatory authorities to maintain trial quality and readiness for inspections.

Matching Summary

The Monitor ensures that clinical trials are conducted properly, protecting human subjects and verifying data accuracy and compliance with protocols and regulations.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Communication with investigators and vendors
  • Leadership in clinical operations
  • Compliance with GCP and protocols
  • Clinical study data management
  • Site qualification and selection

Nice-to-have

  • Collaboration with external partners
  • Mentoring and training CRAs
  • Process ownership and project participation
  • Conflict resolution skills
  • Sharing best practices

Key Requirements

  • At least 3 years CRA experience
  • Bachelor’s degree in biological science or related field
  • Demonstrated leadership capability
  • Experience negotiating complex site issues
  • Ability to manage multiple protocols and sites
  • Effective communication and negotiation skills

Work Rights

Not specified

Tailored Resume

Cover Letter