Senior Clinical Research Associate
Core
Manage trusted site relationships and perform on-site and remote monitoring activities to support the initiation, conduct, and timely completion of Phase I – IV clinical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
High-quality clinical trial data and robust site execution
Domain
Life sciences / Clinical research
Deliverable
physical/clinical work
Required skills
Site monitoring, ICH/GCP compliance, Protocol management, Site initiation visits, Risk identification, Issue resolution, Cross-functional collaboration, Data integrity management
Preferred skills
Oncology experience, CAR T experience, RLT experience
Technologies
Clinical Trial Management Systems (CTMS)
Responsibilities
Manage assigned sites/networks conducting Phase I–IV protocols; Conduct site initiation visits and deliver ongoing training; Perform continuous on-site/remote monitoring for compliance; Identify risks, resolve issues, and escalate concerns; Collaborate with cross-functional teams to drive efficient study execution; Act as a subject matter expert across study activities when required
Seniority
Senior, hands-on IC