Clinical Research Coordinator, FT Days

PIH Health is a nonprofit, regional healthcare network serving approximately 3 million residents in the Los Angeles County, Orange County, and San Gabriel Valley region. The network includes PIH Health Downey Hospital, PIH Health Good Samaritan Hospital, PIH Health Whittier Hospital, 37 outpatient medical office buildings, a multispecialty medical group, home healthcare services, hospice care, and specialized services in heart, cancer, digestive health, orthopedics, women’s health, urgent care, and emergency services. The organization is nationally recognized for excellence in patient care and patient experience.

About the role

The Clinical Research Coordinator (CRC) manages and coordinates clinical research studies in a hospital setting, ensuring compliance with regulatory requirements and institutional policies. The CRC works closely with principal investigators (PIs), research staff, healthcare providers, and study sponsors to support the implementation and management of clinical trials involving human subjects. This role is critical in the day-to-day execution of clinical trials, including participant recruitment, data collection, compliance monitoring, and regulatory documentation.

Responsibilities

• Manage and coordinate clinical research studies in compliance with regulatory requirements and institutional policies.
• Collaborate with principal investigators (PIs), research staff, healthcare providers, and study sponsors.
• Support the implementation and management of clinical trials involving human subjects.
• Oversee participant recruitment, data collection, compliance monitoring, and regulatory documentation.
• Utilize internet access to manage clinical trials case report forms.

Requirements

• High School Diploma or equivalent GED.
• Minimum 2-3 years of experience working in a hospital or academic medical center.
• Minimum 2-3 years of experience in clinical research.
• Current certificate of Human Subjects Protection and Good Clinical Practice training.
• Knowledge of medical environment and terminology.
• Comprehensive knowledge of protocol design and management, FDA regulations, word processing, and spreadsheets.
• Proficiency with computerized and manual data collection.

Qualifications

• Preferred: Bachelor’s degree or Master’s degree in health sciences or related field.
• Preferred: Certification as a Clinical Research Coordinator (e.g., ACRP-CCRC or SOCRA-CCRP).

Pay

$28.81–$49.19 per hour.

Schedule

Days.

Location: 12401 Washington Blvd., Whittier, CA 90602.