Regulatory Coordinator - Los Angeles, CA

The Los Angeles Cancer Network provides unparalleled care to each patient. Its mission is to educate and support patients and their families. It delivers a unique approach for every patient using recent advances in cancer care. · Coordinate regulatory documentation and compliance ...

The Lead Regulatory Coordinator prepares and submits large and/or complex protocols and supporting documentation to regulatory bodies. · Prepares continuations/amendments for compliance. · Advises on workflow within unit/consults staff on new trials. · ...

The Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, and reporting on the various status of research tasks in accordance with FDA guidelines, · Collec ...

The Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, and reporting on the various status of research tasks in accordance with FDA guidelines, ICH GCP ...

The Regulatory Coordinator I is responsible for preparing regulatory research documents in accordance with FDA guidelines. They must maintain regulatory documents and coordinate investigator training. · ...

The Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, · and reporting on the various status of research tasks in accordance with FDA guidelines, · IIC ...

The Regulatory Coordinator maintains accurate paper-based regulatory files for all clinical studies and performs various tasks related to document preparation, updates, and compliance checks. · ...

The Regulatory Coordinator I is responsible for the preparation and implementation of regulatory research documents according to FDA guidelines. · ...

The Regulatory Coordinator is responsible for maintaining accurate paper-based regulatory files for all clinical studies and ensuring compliance with applicable guidelines and site SOPs. · Maintain accurate paper-based regulatory files. · Perform catch-up work on backlogged studi ...

The Lead Regulatory Coordinator prepares and submits large and/or complex protocols and supporting documentation to regulatory bodies and research committees involved in the pre-award and post-award process. · Prepares and submits continuations and amendments to ensure compliance ...

Supports resolution of regulatory complaints and conducts operational audits on Member Experience departments. · ...

The Lead Regulatory Coordinator prepares and submits large and/or complex protocols and supporting documentation to regulatory bodies and research committees involved in the pre-award and post-award process. · ...

The Study Regulatory Coordinator leads regulatory processes across multiple studies of different therapeutic areas and phases. · ...

+The Study Regulatory Coordinator leads regulatory processes across multiple studies in accordance with appropriate regulations and study specific protocols/plans.+ · +Essential Functions & Responsibilities:Manages regulatory activities for all stages of clinical trials. · Mainta ...

This is a full-time on-site role based in City of Industry CA. The Food Quality/ Regulatory Coordinator will be responsible for ensuring regulatory compliance and preparing regulatory documentation. · ...

+Ensure regulatory compliance, prepare and manage regulatory documentation, handle submissions for approval. · +Review and organize daily production and quality documentation · Maintain required records for internal and third-party audits · ...

+Job Summary: · The Assistant Regulatory Affairs Coordinator will work directly with the lead Regulatory Affairs Coordinator to ensure successful management of the regulatory aspects of each study. · +Prepare and/or collect study-related regulatory documents required by IRB, FDA ...

The Assistant Regulatory Affairs Coordinator will work directly with the lead Regulatory Affairs Coordinator to ensure successful management of the regulatory aspects of each study. · ...

We are seeking a detail-oriented professional with dual expertise in clinical research pharmacy operations and regulatory submissions. · ...

+Job summary · Pictor Labs' Clinical Research Associate will play a critical role in supporting research execution, logistics, and operational coordination for virtual staining R&D and clinical evidence generation programs.+Coordinate cross-functional efforts across laboratory, c ...