Entry-Level Clinical Research Associate – Cardiac Trials

Cedars-Sinai; Los Angeles (CA); Presencial; USD 60.000 - 85.000; Jornada completa

Descripción de la vacante

Cedars-Sinai in Los Angeles seeks a Clinical Research Associate I/CPT to support coordination of noncomplex studies under supervision. You will perform data collection, prescreening, and assist with regulatory tasks while ensuring regulatory compliance and data integrity.

Responsibilities include completing CRFs, entering data into EDCs, aiding IRB submissions, and supporting budgets and sponsor communications as part of a multidisciplinary team.

Formación

• Bachelor's degree preferred; CPT- Phlebotomy Certification license required
• High school diploma or GED is required
• 1 year clinical research experience preferred
• Experience supporting IRB submissions and budgeting is a plus

Responsabilidades

• Works under supervision to assist in coordinating noncomplex research studies
• Collects, evaluates and abstracts clinical research data; enters data into EDC systems
• Completes Case Report Forms (CRFs) and assists with prescreening of participants
• Schedules visits and procedures; provides patient contact for follow-up where applicable
• Assists with regulatory submissions to IRB and with budget and billing activities

Conocimientos

Data collection

IRB submissions

HIPAA compliance

EDCs

Participant screening

Educación

High school diploma

Bachelor's degree in Science or related

Herramientas

EDCs

Descripción del empleo

Cedars-Sinai in Los Angeles seeks a Clinical Research Associate I/CPT to support coordination of noncomplex studies under supervision. You will perform data collection, prescreening, and assist with regulatory tasks while ensuring regulatory compliance and data integrity.

Responsibilities include completing CRFs, entering data into EDCs, aiding IRB submissions, and supporting budgets and sponsor communications as part of a multidisciplinary team.