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ICH-GCP
Responsibilities:
- Lead day-to-day oversight of third-party vendors throughout clinical study lifecycle.
- Develop study-specific vendor management plans and monitor vendor performance.
- Facilitate cross-functional collaboration and ensure compliance with GCP and regulatory requirements.
Requirements:
- At least 2 years of experience in Clinical Operations or Vendor Management.
- Proven experience managing third-party vendors and developing oversight plans.
- Strong project management, stakeholder management, and risk assessment skills.
Benefits:
- Fully remote work opportunity based in Brazil.
- Opportunity to collaborate with global clinical research teams.
- Professional growth opportunities in clinical operations and vendor management.
Not Disclosed
The company is a clinical research organization that manages clinical trials and third-party vendors. The team size is not specified, but the culture is collaborative and quality-focused.