Clinical Trials Research Coordinator

University of Southern California; Arcadia (CA); On-site; USD 46,838 - 77,145; Full time

Job summary

University of Southern California in Arcadia is seeking a Research Coordinator to assist in organizing and scheduling assessments to meet study objectives and ensure protocol compliance. You will communicate with study personnel, subjects, IRB and sponsor to support all study activities.

The role involves data collection, regulatory documentation, and collaboration with investigators and external providers, ensuring accurate records and adherence to GCP/HIPAA standards.

Qualifications

• Bachelor's Degree; combined experience/education acceptable.
• Minimum 2 years administrative or research experience.
• Knowledge of medical environment and terminology would be preferred.
• Demonstrated effective communication and writing skills.
• Ability to multi-task and prioritize; work well in a team or independently.

Responsibilities

• Assist with organizing and scheduling assessments/tests/activities to meet research objectives and protocol.
• Serve as contact for subjects, study personnel, IRB and sponsor.
• Coordinate participant recruitment, screening, orientation and appointments.
• Maintain accurate records and regulatory documents.
• Assist in grant proposals and interface with funding/regulatory agencies.
• Support submission of continuing reviews, amendments, and reportable events to IRB.

Skills

Communication skills

Written communication

Multitasking

Teamwork

Clinical documentation

Regulatory knowledge

Education

Bachelor's Degree

Tools

MS Office

Job description

University of Southern California in Arcadia is seeking a Research Coordinator to assist in organizing and scheduling assessments to meet study objectives and ensure protocol compliance. You will communicate with study personnel, subjects, IRB and sponsor to support all study activities.

The role involves data collection, regulatory documentation, and collaboration with investigators and external providers, ensuring accurate records and adherence to GCP/HIPAA standards.