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City of Hope · 4 hours ago

Clinical Study Coordinator

Duarte, CA

Full-time

Onsite

Entry, Mid Level

$41/hr - $64/hr

2+ years exp

City of Hope is a transformative organization focused on fighting cancer and other life-threatening illnesses. They are seeking a full-time Clinical Study Coordinator to support oncology clinical trials, involving patient recruitment, informed consent, and trial coordination.

AssociationEducationHealth Care

Comp. & Benefits

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, and maintain necessary certifications and licensure

Qualification

Clinical trial regulationsACRP certificationSOCRA certificationClinical Practice (GCP)Human Subjects Protection (HSP)Basic Life Support (BLS)Patient recruitmentData managementOrganizational skillsCommunication skillsCollaboration skills

Required

Bachelor's degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education

Minimum of 2 years research or relevant clinical experience

ACRP or SOCRA certification within 1 year of employment

International Air Transport Association (IATA) within 1 month of employment

Good Clinical Practice (GCP) within 1 month of employment

Human Subjects Protection (HSP) within 1 month of employment

Basic Life Support (BLS) within 1 month of employment