University of Southern California
Research Coordinator II
University of Southern California, Los Angeles, California, United States, 90079
Job Title and Employer
Research Coordinator II
– University of Southern California, USC Norris Comprehensive Cancer Center, Clinical Investigations Support Office (CISO).
Job Summary Provide clinical research coordination for oncology protocols; lead study operations, patient enrollment, data management, and regulatory compliance; serve as liaison among investigators, patients, and hospital staff.
Key Responsibilities
Review new protocols prior to CIC approval; assess feasibility and budget impact.
Plan and staff study operations; establish timelines and resource requirements.
Guide investigators, study personnel, and patients in protocol compliance.
Ensure timely and accurate data entry (iSTAR, CAF, CRFs, etc.).
Conduct ongoing assessment of protocol deviations and report SAE to IRB, FDA, and sponsor.
Participate in audits and interact with monitors/auditors from sponsoring pharmaceutical companies.
Maintain drug safety and inventory; coordinate investigational drug logistics with Research Pharmacy.
Schedule and coordinate patient visits, procedures, and specimen collection, including CTU admissions when required.
Assist with training and mentoring of junior coordinators; provide study results to investigators.
Maintain patient care records; support patient interaction, adverse event reporting, and psychosocial assessment.
Collaborate with hospital staff (nurses, social workers, home health) to resolve study-related concerns.
Ensure timely completion of research order forms and billing documentation.
Provide coverage and coordination during absences, ensuring continuity of study operations.
Qualifications
Bachelor’s degree; 2+ years of administrative or research experience; knowledge of medical environment and terminology.
Prior experience as a protocol coordinator in clinical oncology research.
Strong medical background; foreign medical graduate desirable.
Independence and minimal supervision; excellent communication and teamwork across disciplines.
Completion of Human Subject Training, HIPAA, GCP, and Sexual Harassment online courses.
Proficiency with MS Office and ability to manage multiple tasks.
Preferred Experience and Skills
Experience in health and medical services, laboratory, or research settings.
Experience with investigational drug handling, clinical trial logistics, and FDA regulations.
Knowledge of NCI guidelines and sponsor audit expectations.
Salary and Benefits Hourly rate: $35.03 – $43.79. USC offers comprehensive benefits consistent with institutional policies.
Location Los Angeles, California – USC Norris Comprehensive Cancer Center and LAC General Medical Center sites.
EEO Statement USC is committed to equal employment opportunity and encourages applicants of all backgrounds to apply.
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– University of Southern California, USC Norris Comprehensive Cancer Center, Clinical Investigations Support Office (CISO).
Job Summary Provide clinical research coordination for oncology protocols; lead study operations, patient enrollment, data management, and regulatory compliance; serve as liaison among investigators, patients, and hospital staff.
Key Responsibilities
Review new protocols prior to CIC approval; assess feasibility and budget impact.
Plan and staff study operations; establish timelines and resource requirements.
Guide investigators, study personnel, and patients in protocol compliance.
Ensure timely and accurate data entry (iSTAR, CAF, CRFs, etc.).
Conduct ongoing assessment of protocol deviations and report SAE to IRB, FDA, and sponsor.
Participate in audits and interact with monitors/auditors from sponsoring pharmaceutical companies.
Maintain drug safety and inventory; coordinate investigational drug logistics with Research Pharmacy.
Schedule and coordinate patient visits, procedures, and specimen collection, including CTU admissions when required.
Assist with training and mentoring of junior coordinators; provide study results to investigators.
Maintain patient care records; support patient interaction, adverse event reporting, and psychosocial assessment.
Collaborate with hospital staff (nurses, social workers, home health) to resolve study-related concerns.
Ensure timely completion of research order forms and billing documentation.
Provide coverage and coordination during absences, ensuring continuity of study operations.
Qualifications
Bachelor’s degree; 2+ years of administrative or research experience; knowledge of medical environment and terminology.
Prior experience as a protocol coordinator in clinical oncology research.
Strong medical background; foreign medical graduate desirable.
Independence and minimal supervision; excellent communication and teamwork across disciplines.
Completion of Human Subject Training, HIPAA, GCP, and Sexual Harassment online courses.
Proficiency with MS Office and ability to manage multiple tasks.
Preferred Experience and Skills
Experience in health and medical services, laboratory, or research settings.
Experience with investigational drug handling, clinical trial logistics, and FDA regulations.
Knowledge of NCI guidelines and sponsor audit expectations.
Salary and Benefits Hourly rate: $35.03 – $43.79. USC offers comprehensive benefits consistent with institutional policies.
Location Los Angeles, California – USC Norris Comprehensive Cancer Center and LAC General Medical Center sites.
EEO Statement USC is committed to equal employment opportunity and encourages applicants of all backgrounds to apply.
#J-18808-Ljbffr