🛠 Tech Stack

💼 About This Role

You'll support clinical operations for a Chronic Kidney Disease (CKD) pipeline and collaborate with internal teams, CROs, and vendors to ensure smooth trial execution. You'll drive study execution, oversee vendor and site management, and contribute to key study materials. This role offers the chance to take ownership of critical trial activities in a fast-paced precision medicine environment.

🎯 What You'll Do

• Oversee and monitor conduct of global Phase 2 CKD study
• Lead site management oversight and CRO compliance
• Assist in design and development of study documents
• Oversee Trial Master File (TMF) activities

📋 Requirements

• Bachelor's degree with 2-3+ years of clinical operations experience in biotech/pharma
• Familiarity with clinical trial databases such as Medidata Rave or Veeva
• Strong computer proficiency in Microsoft Office Suite
• Willingness to travel 10-15%