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

Trzdev37

Osaka, , Japan
Clinical trial monitoring
Site management and quality assurance
Communication with study teams and vendors
The Monitor ensures that clinical trials are conducted properly, protecting human subjects and verifying data accuracy in compliance with protocols and regulations

Job Summary

  • The Monitor ensures that clinical trials are conducted properly, protecting human subjects and verifying data accuracy in compliance with protocols and regulations.
  • Senior CRAs lead and mentor other CRAs, manage multiple sites and protocols, and contribute to clinical operations projects and initiatives.
  • The role requires strong communication, negotiation, leadership skills, and the ability to collaborate effectively with investigators, CROs, and regulatory authorities.

Matching Summary

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

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • Site management and quality assurance
  • Communication with study teams and vendors
  • Leadership in clinical operations
  • Regulatory compliance and GCP adherence
  • Data accuracy and source verification

Nice-to-have

  • Collaboration with external partners
  • Mentoring and training CRAs
  • Process ownership and project participation
  • Conflict resolution skills
  • Experience with multiple protocols

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 clinical study data delivery
  • Career level D (Senior CRA) or C (CRA)

Work Rights

Not specified

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