Clinical Research Associate I - Breakthrough Trials

Cedars-Sinai; Los Angeles (CA); Presencial; USD 65 000 - 90 000; Tempo integral

Resumo da oferta

Cedars-Sinai is seeking a Clinical Research Associate I to work with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement studies. The role includes data abstraction, CRF completion, and regulatory submissions under HIPAA guidelines.

The candidate will ensure protocol compliance, assist with budget and patient billing, and provide limited patient contact for follow-up as required. Strong attention to detail and GCP knowledge are desirable.

Qualificações

• Education: High School Diploma required; Bachelor's degree preferred in Science, Sociology, or related field.
• One (1) year of clinical research related experience is preferred.

Responsabilidades

• Coordinate/implement study with Clinical Research Coordinator, Research Program Administrator, or Research Nurse.
• Evaluate and abstract clinical research data from source documents.
• Ensure compliance with protocol and clinical research objectives.
• Complete Case Report Forms (CRFs) and enter data into Electronic Data Systems (EDCs).
• Provide supervised patient contact for long-term follow-up as needed.
• Assist with regulatory submissions to the IRB and with study budgets and patient research billing.
• Schedule patients for research visits and procedures; maintain sample preparation and shipping.

Formação académica

High School Diploma

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

Descrição da oferta de emprego

Cedars-Sinai is seeking a Clinical Research Associate I to work with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement studies. The role includes data abstraction, CRF completion, and regulatory submissions under HIPAA guidelines.

The candidate will ensure protocol compliance, assist with budget and patient billing, and provide limited patient contact for follow-up as required. Strong attention to detail and GCP knowledge are desirable.