Clinical Research Associate II - Barcelona
Core
Monitoring clinical trial sites for Gynecologic Oncology or Onco-Hematology studies, ensuring data integrity, patient safety, and regulatory compliance.
Role type
Clinical Research Associate II (IC)
Builds
Clinical trial data and site management for oncology studies
Domain
Biopharmaceuticals / Clinical Research / Oncology
Required skills
Clinical site monitoring, Source document review, CRF review and query resolution, SAE tracking, Regulatory compliance (ICH GCP), Site management, Vendor liaison, Data quality assurance, Protocol adherence verification, Registry management
Preferred skills
Feasibility work, Quality Control Visit participation, Investigator recruitment support, Budget management assistance
Technologies
Clinical trial data management systems, Computer packages
Responsibilities
Conduct routine and closeout monitoring visits, Verify informed consent and protocol adherence, Review source documents and CRFs, Track and report Serious Adverse Events, Manage clinical trial site registries, Liaise with vendors and internal work groups, Prepare trip reports and regulatory submissions
Seniority
Mid-level, hands-on IC