Clinical Research Regulatory Coordinator II - Boston, MA

+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 ...

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 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 (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 ...

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 ...

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

The Regulatory Affairs Coordinator is responsible for supporting the creation and maintenance of labelling projects to enable worldwide regulatory submissions. They prepare and maintain tracking sheets, coordinate the delivery of compliant documentation, and guide experts with re ...

The Regulatory Coordinator performs multiple tasks in order to meet compliance requirements in research. This position will be overseeing clinical research regulatory requirements for the department. · ...

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 the organization's product label and SDS documents systematically organizing them ensuring accuracy and compliance with regulations performing various tasks including providing administrative support to the regulatory ...

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 ...

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. ...

This role is part of ZOLL's Post Market Surveillance and Regulatory reporting program. ...

This role is part of ZOLL's Post Market Surveillance and Regulatory reporting program. · The person will be instrumental in meeting Post Market Surveillance obligations surrounding submissions involving ZOLL devices domestically. · There will be interdepartmental interactions inv ...

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 ...

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

This role is part of ZOLL's Post Market Surveillance and Regulatory reporting program. · Maintain ZOLL's Post Market Surveillance documentation per ZOLL proceduresand Regulatory requirements to stand on its own in the event of an audit. · Identification of complaintsand determina ...

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 ...

This role will be coordinating work across 2 major initiatives related to IDMP and introducing underlying infrastructure services. · ...