Clinical Research Associate I - Heart Institute - Makkar Lab at Cedars-Sinai Los Angeles, CA

Itlearn360; Los Angeles (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Cedars-Sinai's Smidt Heart Institute is looking for a Clinical Research Associate I to support innovative research efforts. The role involves coordinating clinical studies, managing data compliance, and assisting with regulatory processes in a top-tier medical institution dedicated to transformative patient care.

Qualifications

• High School Diploma required, Bachelor's preferred.
• 1 year of clinical research experience preferred.
• Excellent communication skills.

Responsibilities

• Coordinate clinical research studies and ensure compliance.
• Evaluate and abstract data from source documents.
• Support regulatory submissions and manage study samples.

Skills

Communication

Data Evaluation

Regulatory Knowledge

Education

High School Diploma

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

Job description

Clinical Research Associate I - Heart Institute - Makkar Lab Job at Cedars-Sinai, Los Angeles, CA

Job Description

Join Cedars-Sinai's Smidt Heart Institute, a leader in heart disease research and patient care. We are seeking a Clinical Research Associate I to support our groundbreaking research efforts.

The role involves working closely with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and implement clinical studies. Responsibilities include evaluating and abstracting research data, ensuring compliance with protocols, completing case report forms, entering data into electronic systems, assisting with regulatory submissions, and supporting study budgets and patient billing. The position may involve limited patient contact, primarily for study follow-up.

Primary Duties & Responsibilities

• Coordinate and implement clinical research studies
• Evaluate and abstract data from source documents
• Ensure compliance with study protocols and objectives
• Complete Case Report Forms (CRFs)
• Enter data into Electronic Data Systems (EDCs)
• Assist with regulatory submissions to IRB, including adverse event reporting
• Support study budgets and patient billing processes
• Schedule research visits and procedures
• Manage study samples, supplies, and shipping
• Maintain compliance with FDA, IRB, and HIPAA regulations
• Follow Good Clinical Practice (GCP) guidelines
• Maintain patient confidentiality
• Participate in training and education programs

Qualifications

• High School Diploma required; Bachelor's degree preferred in Science, Sociology, or related field
• No experience required; 1 year of clinical research experience preferred
• Ability to interpret regulations and apply knowledge accordingly
• Excellent communication skills

About Cedars-Sinai

Cedars-Sinai is a renowned healthcare provider and research institution committed to innovative patient care and medical advancements. Since 1902, we have served diverse communities and led in healthcare transformation.

Team and Work Environment

Join one of the largest nonprofit academic medical centers in the U.S., offering a fast-paced environment dedicated to high-quality care and research.