🛠 Tech Stack

💼 About This Role

You'll lead global study start-up activities for complex clinical trials, ensuring investigative sites are activated on time. You'll drive activation strategies across regulatory, feasibility, and operational teams. This role directly accelerates patient access to new therapies in a fast-paced, collaborative environment.

🎯 What You'll Do

• Coordinate cross-functional teams for study start-up execution
• Manage site activation timelines and milestones in project systems
• Lead start-up meetings, risk assessments, and escalation management
• Oversee critical path for submissions, contracts, and supply logistics

📋 Requirements

• 5–7+ years in clinical research or study start-up
• Global clinical trial operations across multiple regions
• GCP and regulatory process expertise
• Project management with enterprise tools and dashboards

✨ Nice to Have

• Advanced degree (MS/PhD) in scientific field
• Experience in oncology, vaccines, or rare diseases

🎁 Benefits & Perks

• 💰 Competitive compensation
• 🏥 Health, dental, and vision insurance
• 🌍 Global exposure across therapeutic areas
• 🏠 Remote or hybrid work flexibility
• 📚 Professional development opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Panel Interview· 60 min