13h ago
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Regulatory Coordinator I - Neurosciences - Los Angeles, CA

United StatesUnited States·Los Angelesmid
OtherCoordinator
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Quick Summary

Key Responsibilities

Submits continuations and amendments as necessary to maintain compliance with regulatory requirements and institutional policies.

Technical Tools
OtherCoordinator
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps.

Job Description
Are you ready to bring your skills to a world-class healthcare organization recognized as one of the top ten in the United States? Come join our team!

About the Role

This position will provide support to the Departments of Neurology and Neurosurgery at Cedars-Sinai Medical Center.

The Regulatory Coordinator I prepares and submits protocols and supporting documents to regulatory bodies such as PPC, PRMC, IBCS, Cedars-Sinai IRB, External IRB, IACUC and any research committee involved in the Pre-Award/Post-award process. This role submits continuations, amendments, responds to questions, generates reports, and maintains research files and documentation involving the regulatory requirements for the study/clinical trial. Other duties include, representing the Research Department when meeting with sponsors, attending team meetings, and working with other staff to ensure all regulatory documents and requirements are up-to-date. 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:

Submits continuations and amendments as necessary to maintain compliance with regulatory requirements and institutional policies.
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study.
Completes forms and generates all reports necessary to follow regulatory requirements and institutional policies.
Works closely with the clinical trial coordinator, research staff, and investigators to make sure that all regulatory documents for the research studies are up-to-date.
Attends research team meetings and updates staff and investigators on the status of regulatory submission and amendments.
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.

Responsibilities

~1 min read
Qualifications
Education, Experience, and Skills:

Bachelor's degree, required.
One (1) year minimum of directly related experience is required.
Specialty research certification, preferred.

Minimum Salary
28.86
Maximum Salary
49.06

Location & Eligibility

Where is the job
Los Angeles, United States
On-site at the office
Who can apply
US

Listing Details

Posted
October 9, 2026
First seen
October 9, 2026
Last seen
October 9, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
57%
Scored at
October 9, 2026

Signal breakdown

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Regulatory Coordinator I - Neurosciences - Los Angeles, CA