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Cedars-Sinai · 3 days ago

Clinical Research Coordinator I - Department of Neurology (Hybrid)

Los Angeles, CA

Full-time

Hybrid

Entry Level

$24/hr - $39.76/hr

1+ years exp

Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. The Clinical Research Coordinator I will support the research programs in the Department of Anesthesia and Neurology by coordinating study activities, ensuring compliance with regulations, and maintaining data integrity throughout clinical trials.

CommunitiesHealth CareMedicalNon Profit

Comp. & Benefits

Responsibilities

Scheduling of research participants for research visits and procedures

In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug

Schedules and participates in monitoring and auditing activities

Notifies direct supervisor about concerns regarding data quality and study conduct

Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters following local and federal guidelines

May perform other regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation

Maintains research practices using Good Clinical Practice (GCP) guidelines

Maintains strict patient confidentiality according to HIPAA regulations and applicable law

Participates in required training and education programs

Coordinates training and education of other personnel

Transportation of research medications

Performs research study related assessments and questionnaires

Assists with prescreening of research participants for various clinical trials

Attends research meetings and monthly conference calls with sponsors for study updates

Maintains organized paper and electronic research files

Performs all data collection and data entry tasks for department clinical trials

Assists with preparing manuscripts, letters, and other research documents as needed

Responds to sponsor’ inquiries regarding protocol start-up activities and recruitment

Performs literature reviews

Qualification

Clinical research experienceClinical Practice (GCP)ACRP/SOCRA certificationData collectionPatient confidentialityDocumentation skillsCommunication skills

Required

High School Diploma/GED, required

1 year of clinical research experience, required

Preferred

Bachelor's degree in a Science, Sociology, or related field is preferred

ACRP/SOCRA certification is preferred

Company

Cedars-Sinai

Glassdoor4.0

Since its beginning in 1902, Cedars-Sinai has evolved to meet the healthcare needs of one of the most diverse regions in the nation, continually setting new standards for quality and innovation in patient care, research, teaching and community service.

Founded in 1902

Los Angeles, California, USA

10001+ employees