R&D Sr. Regulatory Coordinator - Newport Beach, CA

· The Irvine Clinical Research site network is the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease ...

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 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 Sr.Regulatory Coordinator supports clinical research teams with minimal direction and considerable use of independent judgment,facilitating study start-up approval process,maintaining documentation of regulatory compliance throughout trial duration. · ...

About Us: · Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatr ...

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 ...

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 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 ...

About Us: · Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatr ...

About Us: · Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry ...

About Us: · Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry ...

Benefits: · 401(k) matching · Dental insurance · Health insurance · Paid time off · Training & development · Vision insurance · Job Summary: · Responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiatio ...

Benefits: · 401(k) matching · Dental insurance · Health insurance · Paid time off · Training & development · Vision insurance · Job Summary: · Responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiati ...

· Benefits:401(k) matching · Dental insurance · Health insurance · Paid time off · Training & development · Vision insurance · Job Summary:   · Responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiat ...

This recruitment is for Temporary Regulatory Affairs Coordinator position through UCI's internal temporary staffing service. · Duties include but are not limited to: Ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical R ...

The Temporary Clinical Regulatory Affairs Coordinator will ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research. · Ensure successful management of the regulatory aspects of each study conducted through UCI's Cen ...

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. · ...

+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 ...

+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 · ...