CRA II/ SCRA
No visa sponsorship
Core
Independent monitoring of oncology clinical trial sites from initiation to close-out, ensuring patient safety, data integrity, and regulatory compliance.
Role type
Senior Clinical Research Associate (IC)
Builds
Clinical trial data and site performance for oncology studies
Domain
Clinical Research / Oncology
Required skills
Independent site monitoring, risk identification, protocol adherence, stakeholder management, regulatory compliance (ICH-GCP), travel management
Preferred skills
Early-phase oncology trial monitoring, CAR-T trial experience, complex study management
Technologies
Clinical trial management systems, electronic data capture platforms
Responsibilities
Manage and monitor investigative sites independently, partner with CTMs to resolve issues, interact with clients for site payments, mentor junior CRAs
Seniority
Senior, hands-on IC
