Clinical Research Regulatory Coordinator II - Boston

The Regulatory Coordinators (RC) works under the direction of the Breast Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research ...

The Regulatory Coordinators works under the direction of the Breast Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of clinical research project. ...

The Regulatory Coordinators works under the direction of the Thoracic Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research pro ...

+The Regulatory Coordinators (RC) works under the direction of the Thoracic Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical resear ...

Job summaryThe Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. · ResponsibilitiesThe Regulatory Coordinator is responsible for the coordination, preparation, and maintenance o ...

We are proud to be a member of the Rentokil family of companies, the global leader in Pest Control and other services across more than 90 countries. We pride ourselves on being a trusted partner to many of the world's leading brands and serve consumer and business customers acros ...

The Regulatory Document Control Coordinator is responsible for organizing product labels and SDS documents ensuring accuracy and compliance with regulations. ...

Serve as the primary point of contact regarding scheduling OTIP observations. · Routinely coordinate communications between all parties involved in the OTIP observation process. · Maintain an electronic log of OTIP observations. Strong organizational and multitasking abilitiesAbi ...

Summary · Works under general supervision to ensure the regulatory requirements for clinical trials are met. · ...

Works under general supervision to ensure the regulatory requirements for clinical trials are met. · This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies. ...

The Clinical Research Regulatory Coordinator I works under general supervision to ensure the regulatory requirements for clinical trials are met. · This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulato ...

The Regulatory Affairs Coordinator II (RAC II) is responsible for the collection, completion and submission of regulatory documents to the clinical trial sponsors and the Institutional Review Board (IRB). ...

The Clinical Research Regulatory Coordinator II is responsible for the collection submission of regulatory documents to clinical trial sponsors and Institutional Review Board IRB.Key responsibilities include facilitating new trial submissions developing informed consent documents ...

The Regulatory Affairs Coordinator II (RAC II) is responsible for the collection, completion and submission of regulatory documents to the clinical trial sponsors and the Institutional Review Board (IRB). · ...

Site: Mass General Brigham IncorporatedMass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teachin ...

· Company Description · Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracte ...

Site: Mass General Brigham Incorporated · Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teac ...

The Regulatory Affairs Coordinator II (RAC II) is responsible for the collection, completion and submission of regulatory documents to the clinical trial sponsors and the Institutional Review Board (IRB). · Facilitate initial new trial submission for SRC and IRB review · Develop ...

The Regulatory Coordinator works collaboratively with Regulatory Specialists to ensure accuracy and compliance of regulatory label content, · claims and 3rd party logos for label design of Private Brands products.This position generates the pack copy from the specification system ...

A Regulatory Document Coordinator is responsible for supporting regulatory dossier authoring and managing document reviews to ensure compliance with internal standards and regulatory requirements. · ...