Teams at Parexel

Provides direct nursing care to participants in early-phase clinical trials. Responsibilities include administering investigational treatments, monitoring participant health, assessing eligibility and symptoms, coordinating laboratory testing, collecting and processing samples, documenting findings, entering clinical data, supporting participant enrollment, and ensuring compliance with SOPs, GCP, and study protocols. The role requires an active California RN license, BLS certification, and ACLS certification within six months of starting.

Onsite bilingual (English/Mandarin) research associate supporting Phase I clinical trials: recruit and screen participants, conduct protocol visits, maintain study logs and supplies, handle samples, assist physicians and monitors, ensure participant safety and data quality, and follow clinical operating and quality management guidelines.

Manages investigator sites throughout clinical trials, from activation through close-out, ensuring patient safety, GCP compliance, protocol adherence, recruitment progress, data quality, investigational product accountability, and timely documentation. Conducts onsite and remote monitoring, resolves site and data issues, supports audits and CAPA activities, addresses adverse event reporting, trains site personnel, and collaborates with study teams, investigators, vendors, and drug safety partners. Requires substantial travel and expertise in clinical research regulations and monitoring.