Clinical Research Coordinator II: Study Management & Data Quality

Hoag Health System; Irvine (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

Hoag Memorial Hospital Presbyterian is seeking a Clinical Research Coordinator II to oversee FDA-regulated trials and sponsor-led studies. The role involves coordinating with physicians, sponsors, and study teams throughout planning, execution, and post-study steps.

The CRC-II manages informed consent, protocol adherence, data collection, and regulatory compliance, ensuring accurate CRFs and timely reporting.

Qualifications

• Excellent verbal and written communications and presentation skills.
• Excellent organizational skills and interpersonal skills to work effectively in a diverse team.
• Attention to details.
• Proficiency with Microsoft Word, PowerPoint, and Windows.
• Excellent analytical and problem-solving skills.
• Ability to work in a fast-paced, team-based environment; project management and coordination skills.
• Ability to establish cooperative working relationships with patients, co-workers, & physicians.

Responsibilities

• Prepare study treatment plans and source documentation, gather study data, and assess subject eligibility.
• Develop protocol-specific assessments and ensure data quality in the study database.
• Host study team meetings, attend site initiation visits, and communicate with sponsors and collaborators.

Skills

Verbal communication

Written communication

Presentation skills

Organizational skills

Interpersonal skills

Team collaboration

Data management

Education

High School Diploma with 2-3 years CRC experience

IATA Certification

ACRP or SoCRA Certification

Tools

Microsoft Word

PowerPoint

Windows

Job description

Hoag Memorial Hospital Presbyterian is seeking a Clinical Research Coordinator II to oversee FDA-regulated trials and sponsor-led studies. The role involves coordinating with physicians, sponsors, and study teams throughout planning, execution, and post-study steps.

The CRC-II manages informed consent, protocol adherence, data collection, and regulatory compliance, ensuring accurate CRFs and timely reporting.