Onsite Clinical Study Coordinator: Oncology Trials

Cancer Treatment Centers of America, Inc.; Duarte, Northern (CA, KY); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

City of Hope seeks a full-time, on-site Clinical Study Coordinator at the Duarte Medical Center to support oncology clinical trials from First in Human to Phase III. You will recruit participants, obtain informed consent, coordinate trials, manage data, and ensure regulatory compliance in a fast-paced environment.

The ideal candidate has a Bachelor’s degree in Science/Health, 2+ years of clinical research experience, and relevant certifications (ACRP/SOCRA, IATA, GCP, HSP, BLS).

Qualifications

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

Responsibilities

• Understand and apply FDA, OHRP, GCP/ICH, HIPAA regulations 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 understanding and compliance.
• Monitor eligibility, safety, and protocol adherence; report adverse events promptly.
• Pursue ongoing education and maintain required certifications/licensure.

Skills

Communication skills

Regulatory knowledge

Attention to detail

Education

Bachelor’s degree in Science/Health or related field

ACRP or SOCRA certification

IATA certification

GCP certification

HSP training

BLS certification

Tools

Regulatory systems

Job description

City of Hope seeks a full-time, on-site Clinical Study Coordinator at the Duarte Medical Center to support oncology clinical trials from First in Human to Phase III. You will recruit participants, obtain informed consent, coordinate trials, manage data, and ensure regulatory compliance in a fast-paced environment.

The ideal candidate has a Bachelor’s degree in Science/Health, 2+ years of clinical research experience, and relevant certifications (ACRP/SOCRA, IATA, GCP, HSP, BLS).