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Cedars-Sinai Clinical Research Coordinator I - Pulmonary Research in Los Angeles, California

Are you looking to contribute to pioneering research? We look forward to having you join our team to collaborate on groundbreaking research!

The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This role is also responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The CRC I member presents study information at regular research staff meetings and ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local. Institutional Review Board (IRB).

Primary Duties and Responsibilities:

•Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.

•Schedules patients for research visits and procedures.

•In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.

•Maintains accurate source documents related to all research procedures.

•Responsible for data collection, documentation, entry, and reporting including timely response to sponsor queries.

•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 in accordance with local and federal guidelines.

•May perform other regulatory 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.

Education:

  • High School Diploma/GED is required

  • Bachelor's Degree in Science, Sociology, or related degree is preferred

Licenses/Certifications:

  • Clinical Research SoCRA or ACRP certification is preferred

Experience:

  • 1 year of clinical research related experience is required

Physical Demands:

Standing, Walking, Sitting, Lifting 50 lbs. Carrying 50 lbs. Pulling 75 lbs. Reaching, Handling, Grasping, Feeling, Talking, Hearing, Repetitive Motions, Eye/Hand/Foot Coordination

Working Title: Clinical Research Coordinator I - Pulmonary Research

Department: Home Dept - Pulmonary

Business Entity: Academic / Research

Job Category: ,Academic/Research,Academic/Research

Job Specialty: Research Studies/Clinical Trials

Position Type: Full-time

Shift Length: 8 hour shift

Shift Type: Day

Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

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