Impactful Oncology Clinical Research Coordinator

aa067; Irvine (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

City of Hope seeks a full-time, on-site Clinical Study Coordinator to support oncology trials. You will coordinate patient recruitment, informed consent, and care, while ensuring regulatory compliance and data integrity across trial phases.

Responsibilities include managing data, monitoring eligibility and safety, and reporting adverse events. The role requires strong collaboration with investigators and sponsors in a fast-paced clinical research setting.

Qualifications

• Bachelor’s degree in Science, Health or related field required; 3 additional years experience may substitute.
• Minimum of 2 years research or relevant clinical experience.
• ACRP or SOCRA certification within 1 year of employment.
• IATA within 1 month of employment.
• GCP within 1 month of employment.
• HSP within 1 month of employment.
• BLS within 1 month of employment.

Responsibilities

• Coordinate patient recruitment, informed consent, and care.
• Manage trial data, regulatory compliance, and documentation.
• Monitor participant eligibility, safety, and protocol adherence; report adverse events.
• Collaborate with investigators, sponsors and clinical staff in a fast-paced environment.

Skills

Regulatory compliance

Coordination

Stakeholder communication

Data management

Clinical trial regulations

Education

Bachelor’s degree in Science, Health or related field

3 additional years of experience may substitute for minimum education

Job description

City of Hope seeks a full-time, on-site Clinical Study Coordinator to support oncology trials. You will coordinate patient recruitment, informed consent, and care, while ensuring regulatory compliance and data integrity across trial phases.

Responsibilities include managing data, monitoring eligibility and safety, and reporting adverse events. The role requires strong collaboration with investigators and sponsors in a fast-paced clinical research setting.