Full-time
Clinical Research Coordinator, FT Days
Competitive
Whittier, CAScience & PharmaceuticalPosted 17d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
17 days ago
Job description
PIH Health Whittier Hospital is hiring a Clinical Research Coordinator to manage and coordinate clinical research studies in a hospital setting while ensuring regulatory and institutional compliance. The role supports clinical trials through participant recruitment, data collection, compliance monitoring, and regulatory documentation.
Responsibilities
The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical research studies conducted 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 position plays a critical role in the day-to-day execution of clinical trials, including participant recruitment, data collection, compliance monitoring, and regulatory documentation
Preferred
Bachelor's degree or Master's degree in health sciences or related field
Certification as a Clinical Research Coordinator (e.g., ACRP-CCRC or SOCRA-CCRP)
Health Sciences
Clinical Research Coordination
Clinical Research Coordinator Certification
Company
Nonprofit regional healthcare network
Whittier, California, USA
https://www.pihhealth.org/
Founded in 1959
5001-10000 employees
Qualifications
Comprehensive knowledge in all areas of protocol design and management, FDA regulations, word processing, spreadsheets and, working knowledge of medical research terminology
Proficient with computerized and manual data collection
Familiarity with word processing and spreadsheet computer programs
High School Diploma or equivalent GED
Minimum 2-3 years working in a hospital or academic medical center
Minimum 2–3 years of experience in clinical research
Must be knowledgeable in internet access to manage clinical trials case report forms
Current certificate of Human Subjects Protection and Good Clinical Practice training
Knowledge of medical environment and terminology
Bachelor's degree or Master's degree in health sciences or related field
Certification as a Clinical Research Coordinator (e.g., ACRP-CCRC or SOCRA-CCRP)
Required skills
Clinical Research, Clinical Research Protocol Design and Management, FDA Regulations, Clinical Practice, Human Subjects Protection, Clinical Trial Case Report Forms, Data Collection, Medical Terminology, ACRP-CCRC, SOCRA-CCRP
Preferred skills
Glassdoor, 3.7, PIH Health is a nonprofit, regional healthcare network., Whittier, California, USA, https://www.pihhealth.org, Late Stage, Leadership Team, Charlotte A. Weaver, Lydia Arroyo, Chief Nursing Officer, Recent News, PR Newswire, 2026-07-10, 2026-04-15, Morningstar.com, PIH Health, Inc. Media Statement Regarding Data Event, 2026-03-07, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness
Experience
2-3 years
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