Entry-Level Clinical Research Associate — Breakthrough Trials

Cedars-Sinai; Los Angeles (CA); In loco; USD 70.000 - 90.000; Tempo pieno

Descrizione del lavoro

Cedars-Sinai Medical Center is seeking a Clinical Research Associate I to support coordination of noncomplex studies under supervision. You will assist with data collection, participant scheduling, IRB tasks, and regulatory compliance within a dynamic research environment.

The role involves sample handling, budget assistance, and ensuring adherence to Good Clinical Practice while maintaining patient confidentiality in line with HIPAA regulations.

Competenze

• Education requirements: High School Diploma or GED; Bachelor’s degree preferred.
• Experience: 1 year clinical research experience preferred.

Mansioni

• Coordinate/implement study with CRAs, coordinators or nurses.
• Abstract and evaluate clinical research data from source documents.
• Ensure protocol compliance with study objectives.
• Complete Case Report Forms (CRFs).
• Enter data into sponsor-provided EDC systems.
• Assist with IRB submissions and regulatory tasks.
• Assist with clinical trial budgets and patient research billing.
• Pre-screen potential research participants and schedule visits.

Conoscenze

Data collection

Participant scheduling

Regulatory compliance

IRB submissions

GCP compliance

Formazione

High School Diploma/GED

Bachelor's degree in Science, Sociology, or related field

Strumenti

EDC systems

Descrizione del lavoro

Cedars-Sinai Medical Center is seeking a Clinical Research Associate I to support coordination of noncomplex studies under supervision. You will assist with data collection, participant scheduling, IRB tasks, and regulatory compliance within a dynamic research environment.

The role involves sample handling, budget assistance, and ensuring adherence to Good Clinical Practice while maintaining patient confidentiality in line with HIPAA regulations.