Clinical Research Coordinator Full time Days
PIH Health, South El Monte, CA, United States
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.
Required Skills
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.
Required Experience
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.
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).
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.
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Required Skills
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.
Required Experience
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.
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).
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.
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