Added
3 minutes ago
Type
Full time
Salary
Salary not provided

Related skills

gcp budgeting ich regulatory compliance
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📋 Description

  • Oversee clinical trial management activities: site management, monitoring, and data integrity.
  • Manage site interactions from activation to closeout, including recruitment and payments.
  • Identify risks to timelines, quality, budget; develop mitigation strategies.
  • Review protocols, budgets, and contracts; ensure clear expectations.
  • Lead study meetings with updates and recommendations.
  • Escalate site challenges and resolve operational issues.

🎯 Requirements

  • Bachelor’s degree, nursing (RN), or related field in clinical research.
  • Proven experience in managing clinical trials (site/monitoring).
  • Ability to lead teams and coordinate stakeholders toward milestones.
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Experience with international research environments and risk-based monitoring.
  • Experience managing budgets, timelines, and study delivery.

🎁 Benefits

  • Fully remote full-time position based in Brazil.
  • Work with international teams and professionals in life sciences.
  • Career development through training and mentorship.
  • Collaborative and inclusive work environment.
  • Exposure to innovative technologies and data-driven solutions.
  • Resources to support long-term career progression.
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