Oncology Clinical Research Coordinator

Cancer Treatment Centers of America, Inc.; Irvine (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

City of Hope is seeking a Clinical Study Coordinator in California to support oncology clinical trials from First in Human to Phase III. You will coordinate recruitment, informed consent, data management, and regulatory compliance while collaborating with investigators and clinical staff in a fast-paced environment.

The role requires knowledge of FDA regulations, GCP/ICH, HIPAA, and institutional policies, along with strong organizational and communication skills.

Qualifications

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

Responsibilities

• Understand and 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 to ensure clear understanding and compliance.
• Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
• Pursue continuous education and training opportunities, staying updated with the latest clinical research information.

Skills

Strong organizational skills

Regulatory compliance

Patient communication

Education

Bachelor’s degree in Science, Health or related field

3 years experience may substitute for education

ACRP certification

SOCRA certification

IATA certification

GCP certification

HSP certification

BLS certification

Job description

City of Hope is seeking a Clinical Study Coordinator in California to support oncology clinical trials from First in Human to Phase III. You will coordinate recruitment, informed consent, data management, and regulatory compliance while collaborating with investigators and clinical staff in a fast-paced environment.

The role requires knowledge of FDA regulations, GCP/ICH, HIPAA, and institutional policies, along with strong organizational and communication skills.