On-Site Oncology Clinical Research Coordinator

City of Hope; Duarte (CA); Hybrid; USD 65,000 - 90,000; Full time

Job summary

City of Hope's Duarte Medical Center is seeking a full-time, on-site Clinical Study Coordinator to support oncology trials. Under supervision, you will coordinate First in Human to Phase III and Investigator-Initiated trials, including patient recruitment, consent, and data management.

The role requires strong knowledge of FDA regulations, GCP/ICH, HIPAA, and the ability to collaborate with investigators and staff in a fast-paced environment.

Qualifications

• Bachelor’s degree in Science, Health or related field; 3 additional years of experience may substitute for minimum education.
• Minimum of 2 years research or relevant clinical experience.
• ACRP or SOCRA certification within 1 year of employment.
• IATA certification 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 participant recruitment, informed consent, and care.
• Follow and apply clinical trial protocols and procedures.
• Monitor participant eligibility, safety, and protocol adherence; report adverse events.
• Communicate with investigators, sponsors, and participants to ensure understanding and compliance.
• Ensure data management and regulatory compliance across trials.

Skills

Regulatory knowledge

Informed consent

Coordination skills

Education

Bachelors in Science/Health

Job description

City of Hope's Duarte Medical Center is seeking a full-time, on-site Clinical Study Coordinator to support oncology trials. Under supervision, you will coordinate First in Human to Phase III and Investigator-Initiated trials, including patient recruitment, consent, and data management.

The role requires strong knowledge of FDA regulations, GCP/ICH, HIPAA, and the ability to collaborate with investigators and staff in a fast-paced environment.