On-Site Clinical Research Coordinator Oncology Trials

aa067; Duarte (CA); On-site; USD 70,000 - 100,000; 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. This patient-facing role involves coordinating First in Human to Phase III trials, handling recruitment, consent, data management, and regulatory compliance in a fast-paced clinical environment.

The successful candidate will apply FDA, HHS, and ICH-GCP guidelines, maintain certifications, and collaborate with investigators and staff to ensure protocol adherence and

Qualifications

• Bachelor’s degree in Science, Health or related field from an accredited university.
• 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 within 1 month of employment.
• GCP within 1 month of employment.
• Human Subjects Protection (HSP) within 1 month of employment.
• Basic Life Support (BLS) within 1 month of employment.

Responsibilities

• Apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
• Follow and execute clinical trial protocols and procedures.
• Coordinate participant recruitment, informed consent, and care.
• Communicate with participants, investigators, and sponsors for clarity and compliance.
• Monitor eligibility, safety, and protocol adherence; report adverse events promptly.
• Pursue ongoing education and maintain certifications.

Skills

Regulatory knowledge

Project coordination

Effective communication

Team collaboration

Education

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

Tools

ACRP/SOCRA certification

IATA certification

GCP certification

HSP certification

BLS certification

Job description

City of Hope’s Duarte Medical Center is seeking a full-time, on-site Clinical Study Coordinator to support oncology trials. This patient-facing role involves coordinating First in Human to Phase III trials, handling recruitment, consent, data management, and regulatory compliance in a fast-paced clinical environment.

The successful candidate will apply FDA, HHS, and ICH-GCP guidelines, maintain certifications, and collaborate with investigators and staff to ensure protocol adherence and