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Role Overview:
- Manage clinical trials with focus on quality, timelines, and finances.
- Work remotely in Brazil with international teams.
Key Responsibilities:
- Oversee compliance with ICH-GCP and regulatory standards.
- Lead study teams and coordinate with sites and stakeholders.
- Monitor budgets, resources, and performance metrics.
Qualifications:
- 8+ years in clinical research with trial management experience.
- Strong leadership, planning, and communication skills.
Benefits:
- Fully remote and collaborative environment.
- Opportunities for professional growth and global impact.
Confidential
A clinical research organization specializing in complex clinical trials and regulatory compliance. Offers a collaborative, science-focused, and fully remote work environment with global exposure and professional development opportunities.