"Alerted.org

Job Title, Industry, Employer
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Advanced Search

Advanced Search

Cancel
Remove
+ Add search criteria
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Related to

  • Clinical Research Coordinator I - Pulmonary…

    Cedars-Sinai (Los Angeles, CA)



    Apply Now

    Job Description

    Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!

     

    Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world.

     

    The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The incumbent will be 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 will present study information at 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:

    + 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.

    + 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 / 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.

    Qualifications

    Education:

    + High School Diploma/GED, required.

    + Bachelor's degree, preferred.

    Licenses/Certifications:

    ACRP/SOCRA (or equivalent) certification, preferred.

    Experience:

    1 year of clinical research experience, required.

    About Us

    Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.

    About the Team

    Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.

     

    **Req ID** : 5003

    **Working Title** : Clinical Research Coordinator I - Pulmonary Research Program/Lung Institute

    **Department** : Research - Pulmonary

    **Business Entity** : Cedars-Sinai Medical Center

    **Job Category** : Academic / Research

    **Job Specialty** : Research Studies/ Clin Trial

    **Overtime Status** : NONEXEMPT

    **Primary Shift** : Day

    **Shift Duration** : 8 hour

    **Base Pay** : $23.39 - $39.76

     

    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.

     


    Apply Now



Recent Searches

  • manufacturing engineer machining starship (United States)
[X] Clear History

Recent Jobs

  • Clinical Research Coordinator I - Pulmonary Research Program/Lung Institute
    Cedars-Sinai (Los Angeles, CA)
[X] Clear History

Account Login

Cancel
 
Forgot your password?

Not a member? Sign up

Sign Up

Cancel
 

Already have an account? Log in
Forgot your password?

Forgot your password?

Cancel
 
Enter the email associated with your account.

Already have an account? Sign in
Not a member? Sign up

© 2025 Alerted.org