Hybrid Clinical Research Associate I LA | Data & Compliance

Cedars-Sinai; Beverly Hills (CA); Ibrido; USD 60.000 - 80.000; Tempo pieno

Descrizione del lavoro

Cedars-Sinai in Los Angeles, CA is seeking a Clinical Research Associate I to support coordination of noncomplex studies under supervision. The role involves data collection, screening, scheduling participants, and assisting with regulatory submissions.

Responsibilities include collecting data, completing CRFs, assisting with IRB activities, budgeting, and ensuring compliance with GCP, HIPAA, FDA guidelines. Hybrid work with 4 on-site days per week; commute to LA required.

Competenze

• 1 year of clinical research experience preferred.
• Experience with data collection and entry into EDC systems.
• Familiarity with IRB submissions and regulatory documentation.
• Understanding of HIPAA and GCP guidelines.

Mansioni

• Support coordination and implementation of noncomplex studies.
• Collect and abstract clinical data; assist with CRFs.
• Assist with IRB submissions and safety reporting.
• Support research budgets and patient billing.
• Ensure compliance with FDA, HIPAA, and GCP guidelines.

Conoscenze

Clinical research

Data collection

IRB submission

EDC data entry

Budget and billing

Formazione

High School Diploma/GED

Bachelor's Degree in Science/Sociology or related

Strumenti

Electronic Data Capture (EDC)

Descrizione del lavoro

Cedars-Sinai in Los Angeles, CA is seeking a Clinical Research Associate I to support coordination of noncomplex studies under supervision. The role involves data collection, screening, scheduling participants, and assisting with regulatory submissions.

Responsibilities include collecting data, completing CRFs, assisting with IRB activities, budgeting, and ensuring compliance with GCP, HIPAA, FDA guidelines. Hybrid work with 4 on-site days per week; commute to LA required.