Onsite Clinical Research Coordinator – Oncology Trials
City of Hope
Duarte (CA)
On-site
USD 60,000 - 80,000
Full time
14 days+
Application generator
Stand out for this role — generate a tailored resume and cover letter in about a minute.
Get past ATS filters
Job summary
City of Hope in Duarte, California is hiring a full-time Clinical Study Coordinator. In this patient-facing role, you'll support oncology clinical trials, overseeing patient recruitment, informed consent, and regulatory compliance. You should possess a Bachelor’s degree in Science or Health, alongside 2 years of clinical experience. Certifications in clinical research practices and basic life support are mandatory soon after employment. Become part of a transformative team committed to advancing medical care.
Qualifications
At least 2 years of research or relevant clinical experience required.
ACRP or SOCRA certification needed within 1 year of employment.
IATA, GCP, HSP, and BLS certifications required within 1 month of employment.
Responsibilities
Coordinate participant recruitment and informed consent.
Communicate with participants and ensure compliance.
Monitor and document protocol adherence and report events.
Skills
Knowledge of clinical trial regulations
Strong organizational skills
Ability to collaborate
Education
Bachelor’s degree in Science or Health
Tools
GCP certification
BLS certification
Job description
City of Hope in Duarte, California is hiring a full-time Clinical Study Coordinator. In this patient-facing role, you'll support oncology clinical trials, overseeing patient recruitment, informed consent, and regulatory compliance. You should possess a Bachelor’s degree in Science or Health, alongside 2 years of clinical experience. Certifications in clinical research practices and basic life support are mandatory soon after employment. Become part of a transformative team committed to advancing medical care.