Clinical Trial Manager/Sr Clinical Trial Manager

Erasca, a clinical-stage precision oncology company, seeks a Clinical Trial Manager or Senior Clinical Trial Manager to oversee global oncology trials from planning through completion. The role involves managing clinical vendors, coordinating site relationships, ensuring regulatory compliance, and supporting cross-functional teams in a fast-paced drug development environment.

Responsibilities

• Manage global Phase 1-3 oncology clinical trials in compliance with regulations and GCP
• Recruit and activate study sites; build and maintain investigator relationships
• Oversee vendor selection, contracts, and performance; manage CROs and specialized vendors
• Monitor trial progress including enrollment, material inventory, and data quality
• Develop study protocols, consent forms, regulatory documents, and trial materials

Requirements

• Undergraduate degree in life sciences, pharmacy, medicine, nursing, or allied health
• Minimum 5 years clinical operations experience in oncology (pharmaceutical or CRO)
• Proven trial set-up, monitoring, and close-out experience across Phases 1-3
• Knowledge of ICH-GCP guidelines and FDA regulatory requirements
• Ability to manage multiple vendors, contracts, and timelines
• Experience with clinical trial documentation and eCRF/IRT systems