Entry-Level Clinical Research Associate | Data & Trials Support

Cedars-Sinai; Los Angeles (CA); On-site; USD 65,000 - 75,000; Full time

Job summary

Cedars-Sinai in Los Angeles is seeking a Clinical Research Associate I to support coordination and implementation of noncomplex studies under supervision. You will assist with data collection, prescreening of participants, scheduling visits, and ensuring trial compliance with GCP, HIPAA, and regulatory guidelines.

The role also involves assisting with IRB submissions, budgeting and billing support, sample handling, and serving as a contact for sponsor inquiries under supervision.

Qualifications

• Requires High School Diploma or GED; Bachelor's degree preferred.
• 1 year clinical research related experience preferred.
• No license or certification required.

Responsibilities

• Assists in coordinating noncomplex research studies under supervision.
• Collects, evaluates and abstracts clinical data; enters data into sponsor EDCS.
• Completes Case Report Forms (CRFs) and assists with prescreening of potential participants.
• Schedules visits and research procedures; maintains patient contact for long-term follow-up.
• Assists with IRB submissions and safety reporting per federal and local guidelines.
• Helps with study budgets and participant billing; maintains study supplies and kits.
• Ensures compliance with protocol, GCP, HIPAA, FDA, and IRB requirements.
• May engage with external sponsors and participate in study meetings as directed.

Education

High School Diploma/GED

Bachelor's Degree in Science, Sociology or related degree

Job description

Cedars-Sinai in Los Angeles is seeking a Clinical Research Associate I to support coordination and implementation of noncomplex studies under supervision. You will assist with data collection, prescreening of participants, scheduling visits, and ensuring trial compliance with GCP, HIPAA, and regulatory guidelines.

The role also involves assisting with IRB submissions, budgeting and billing support, sample handling, and serving as a contact for sponsor inquiries under supervision.