Clinical Trial Associate

Responsibilities

• Support clinical trial operations across all phases of the study lifecycle
• Assist with CRO and vendor coordination and oversight
• Collect, track, and review investigator site regulatory documentation
• Manage Trial Master File (TMF) filing, maintenance, and reconciliation
• Track essential study documentation, budgets, and enrollment metrics
• Coordinate study team, vendor, and site meetings
• Support study start-up, conduct, monitoring, and close-out activities
• Assist with site monitoring, audit, and inspection preparation
• Support ordering and distribution of investigational products and study supplies
• Provide operational and financial support including purchase orders and invoice processing
• Assist with development and maintenance of study documents

Requirements

• Bachelor’s degree in a scientific field
• 1-2 years of professional experience in clinical research or equivalent
• Experience with eTMF systems (e.g., Veeva Vault)
• Knowledge of ICH-GCP and current FDA regulations
• Strong organizational and communication skills
• Proficiency in MS Office (Excel, Word, PowerPoint, Outlook, Teams)
• Ability to work in a matrix environment

Preferred Qualifications

• Experience in oncology
• Experience in CRO oversight

About the Company

Kura Oncology is a commercial-stage biopharmaceutical company committed to discovering and developing innovative precision medicines to help patients with cancer lead better, longer lives.