CRC II: Molecular Imaging & Cancer Trials

Hoag Hospital Irvine; Irvine (CA); Hybrid; USD 75.000 - 95.000; Vollzeit

Zusammenfassung

Hoag Memorial Hospital Presbyterian in Irvine, CA seeks a Clinical Research Coordinator II to manage FDA-regulated, industry-sponsored and investigator-initiated trials. Responsibilities include protocol review, informed consent, data management, and coordinating with study physicians and sponsors to ensure compliance and quality.

Requirements include 2–3 years CRC experience, strong communication and organizational skills, and proficiency with MS Word, PowerPoint, and Windows.

Qualifikationen

• 2–3 years of Clinical Research Coordinator experience
• Excellent verbal and written communications, and presentation skills
• Proficiency with Microsoft Word, PowerPoint, and Windows

Aufgaben

• Coordinate FDA regulated industry-sponsored, government funded, and/or investigator initiated trials
• Develop study flow sheets, source documentation, and assess subject eligibility
• Ensure accurate CRFs, SAE reporting, and schedule follow-up visits; maintain data quality

Kenntnisse

Verbal and written communication

Attention to detail

Organizational skills

Interpersonal skills

Project management

Cross-functional collaboration

Tools

Microsoft Word

PowerPoint

Windows

Jobbeschreibung

Hoag Memorial Hospital Presbyterian in Irvine, CA seeks a Clinical Research Coordinator II to manage FDA-regulated, industry-sponsored and investigator-initiated trials. Responsibilities include protocol review, informed consent, data management, and coordinating with study physicians and sponsors to ensure compliance and quality.

Requirements include 2–3 years CRC experience, strong communication and organizational skills, and proficiency with MS Word, PowerPoint, and Windows.