Clinical Research Coordinator: Patient-Focused Trials

CenExel Clinical Research; Riverside (CA); On-site; USD 41,000 - 47,000; Full time

Job summary

CenExel Clinical Research in Riverside, CA is seeking a Clinical Research Coordinator to support coordinating clinical trials in compliance with ICH, GCP, and sponsor requirements. This full-time, on-site role offers a Monday–Friday schedule and a competitive hourly rate.

Responsibilities include coordinating all aspects of patient involvement, organizing trial data, monitoring safety and adverse events, and ensuring accurate documentation and regulatory duties.

Qualifications

• 1+ years of experience as a Clinical Research Coordinator.
• Knowledge of Federal regulations protecting human subjects in research.
• Strong leadership and mentorship skills.
• Ability to work independently and in a team.

Responsibilities

• Assists with coordinating all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.).
• Educates potential participants and caregivers on protocol specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assumes other duties and responsibilities as assigned.

Skills

Clinical Research Coordination

Regulatory knowledge (GCP)

Leadership & mentorship

Communication

Education

Bachelor's Degree

High school diploma or equivalent

Job description

CenExel Clinical Research in Riverside, CA is seeking a Clinical Research Coordinator to support coordinating clinical trials in compliance with ICH, GCP, and sponsor requirements. This full-time, on-site role offers a Monday–Friday schedule and a competitive hourly rate.

Responsibilities include coordinating all aspects of patient involvement, organizing trial data, monitoring safety and adverse events, and ensuring accurate documentation and regulatory duties.