Clinical Research Associate I - Data & Trial Support

Cedars-Sinai; Los Angeles (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

Cedars-Sinai is seeking a Clinical Research Associate I/CPT to support noncomplex clinical studies under supervision. You will assist in data collection, CRF completion, IRB submissions, and budgeting activities, ensuring compliance with GCP and HIPAA standards.

The role involves coordinating participant activities, aiding in regulatory submissions, and maintaining study supplies while working under the direction of experienced staff.

Qualifications

• Proven ability to collect and evaluate clinical data and support study forms.
• Experience with IRB submissions and regulatory documentation.
• Familiarity with HIPAA and Good Clinical Practice (GCP) guidelines.

Responsibilities

• Assist in coordination/implementation of noncomplex studies.
• Collect and enter data into EDC systems; prepare CRFs.
• Assist with prescreening and scheduling participants; support budgets and billing.

Skills

Data collection

IRB submission

Regulatory compliance

Clinical research coordination

Budget support

Education

Bachelor's degree in Science or related field

High school diploma/GED

Tools

EDC systems

Budget tracking tools

Job description

Cedars-Sinai is seeking a Clinical Research Associate I/CPT to support noncomplex clinical studies under supervision. You will assist in data collection, CRF completion, IRB submissions, and budgeting activities, ensuring compliance with GCP and HIPAA standards.

The role involves coordinating participant activities, aiding in regulatory submissions, and maintaining study supplies while working under the direction of experienced staff.