Associate Director, Regional Clinical Study Management

📋 Description

• Lead planning, execution, and delivery of Phase I–IV oncology trials.
• Oversee regional study activities with autonomy; define milestones and timelines.
• Mentor and develop the clinical operations team in Brazil.
• Coordinate protocol execution across sites and partners.
• Manage CROs, vendors, investigators, and external stakeholders.
• Monitor milestones, risks, and escalation processes for study performance.

🎯 Requirements

• Bachelor’s or higher in a scientific/healthcare field; Master’s preferred.
• 10+ years in clinical research; 5+ years in PM/monitoring preferred.
• Experience in pharma/biotech/oncology; knowledge of FDA, ICH/GCP regulations.
• Experience with trial planning, budgeting, CRO/vendor management, and regulatory readiness.
• Strong leadership, communication, and collaboration skills; oncology exposure preferred.
• Willingness to travel ~10–25% as needed.

🎁 Benefits

• Hybrid work model based in São Paulo, Brazil.
• Opportunity to lead regional clinical operations for complex oncology studies.
• Senior-level exposure to global clinical development and cross-functional teams.
• Professional growth through leadership responsibilities and initiatives.
• Work with multidisciplinary internal teams, CROs, investigators, vendors, and external partners.
• Exposure to high-impact clinical research programs and international studies.