Dynamic Clinical Research Coordinator: Trials, Data & Compliance

Keck Medicine of USC; Arcadia (CA); On-site; USD 4,728,000 - 7,741,000; Full time

Job summary

Keck Medicine of USC in Arcadia is seeking a Research Coordinator to support clinical studies by coordinating assessments, scheduling visits, and ensuring protocol compliance. You will serve as a liaison among study teams, subjects, IRB, and sponsors.

Responsibilities include data collection, regulatory documentation, maintaining records, preparing reports, and assisting with grant proposals. A Bachelor's degree and 2 years of administrative or research experience are required.

Qualifications

• Bachelor’s Degree combined experience/education as substitute for minimum education.
• 2 years Administrative or research experience.
• Working knowledge of MS Office applications.
• 2 years Knowledge of medical environment and terminology.

Responsibilities

• Assists with organizing and scheduling assessments/tests/activities to meet research objectives and study protocol compliance.
• Communicates with study team personnel to ensure study procedures are followed and research is performed as described in protocol.
• Serves as contact for subjects, study personnel, IRB and study sponsor.
• Assists with data collection for research studies following established data collection and management procedures.
• Collects, records, enters and prepares data for analysis.
• Performs preliminary study analysis under the direction of the Principal Investigator or senior coordinators.

Skills

Effective communication

Strong writing skills

Multi-tasking

Team collaboration

Clinical documentation

Regulatory knowledge

Education

Bachelor’s Degree

Tools

MS Office

Job description

Keck Medicine of USC in Arcadia is seeking a Research Coordinator to support clinical studies by coordinating assessments, scheduling visits, and ensuring protocol compliance. You will serve as a liaison among study teams, subjects, IRB, and sponsors.

Responsibilities include data collection, regulatory documentation, maintaining records, preparing reports, and assisting with grant proposals. A Bachelor's degree and 2 years of administrative or research experience are required.