Clinical Research Associate 1 day ago $125,000–$150,000/yr US Monitor clinical trial sites to ensure ethical, safe, and compliant conduct per protocol, GCP, and regulations.Serve as primary liaison between Lycia and investigative sites for startup, maintenance, and close-out activities.Manage regulatory documents, EDC data queries, and remote monitoring to maintain audit-ready TMF and CTMS records. Clinical Research GCP EDC CTMS Regulatory Compliance View details Similar jobs