Licensing and Regulatory Specialist - 5866DESCRIPTION/RESPONSIBILITIES: The Producer Services department works to onboard new producer to Chubb. Send all documents via DocuSign * Triage Department Mailboxes to make sure all requests get to the proper specialist or department. Prepare and send termin...
Regulatory Specialist will play an integral part in the regulatory IND submission process of new pharmaceutical products. Maintain regulatory systems and processes including the regulatory submissions and correspondences tracker, Regulatory SharePoint site, and file sharing tools used to interact wi...
The Corporate Information Services Department is seeking a dynamic and talented Senior Clinical Informatics Specialist. Senior Clinical Informatics Specialist. ...
Product Stewardship and Regulatory Affairs Specialist. The Arkema Americas Product Stewardship and Regulatory Affairs team based out of King of Prussia, PA, has an opening for a Sr. In conjunction with each Business Unit for which the position is responsible, this position manages activities to assu...
Independently prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations (CROs), and required governmental agencies, as well as, organize and maintain all regulatory affairs documentation/investigator site files (ISF) as required. Independ...
The Corporate Information Services Department is seeking a dynamic and talented Senior Clinical Informatics Specialist. ...
Regulatory Specialist will play an integral part in the regulatory IND submission process of new pharmaceutical products. Maintain regulatory systems and processes including the regulatory submissions and correspondences tracker, Regulatory SharePoint site, and file sharing tools used to interact wi...
The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. Reviews Document Change Orders for Regulatory compliance, including drawings and labeling ...
Develop awareness of regulatory legislation, guidance and practice in the assigned countries with the support from senior staff•Assist senior staff to compile, prepare, submit and obtain approval of the submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirem...
Independently prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations (CROs), and required governmental agencies, as well as, organize and maintain all regulatory affairs documentation/investigator site files (ISF) as required. Independ...
BDP International, a member of the PSA Group, is a leading provider of global, integrated supply chain, transportation and logistics solutions.The company was founded in by Richard Bolte Sr.Now, BDP employs more than 5, people worldwide and operates freight logistics centers worldwide through a glob...
Product Stewardship and Regulatory Affairs Specialist. The Arkema Americas Product Stewardship and Regulatory Affairs team based out of King of Prussia, PA, has an opening for a Sr. In conjunction with each Business Unit for which the position is responsible, this position manages activities to assu...
Environmental Regulatory Specialist. For the Managing Consultant, Environmental Regulatory Specialist (Senior Level) position, we anticipate the annual base pay of $76,000 – $94,860 (USD). Federal Energy Regulatory Commission (FERC). Research, analyze and compile data for permit applications and rep...
Regulatory Specialist will play an integral part in the regulatory IND submission process of new pharmaceutical products. Maintain regulatory systems and processes including the regulatory submissions and correspondences tracker, Regulatory SharePoint site, and file sharing tools used to interact wi...
Regulatory Operations Specialist. Regulatory Operations Specialist. Regulatory Operations Specialist. Regulatory Operations Specialist. ...
The Corporate Information Services Department is seeking a dynamic and talented Senior Clinical Informatics Specialist. Senior Clinical Informatics Specialist. ...
As a Regulatory Risk Specialist within PNC Investments organization, you will be based in Philadelphia, PA or Bridgewater, NJ. Partners with regulatory risk manager to execute regulatory risk initiatives including setting up, building and monitoring initiatives. Participates in regulatory and audit ...
Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Keeps abreast of regula...
Regulatory Operations Specialist. Regulatory Operations Specialist. Regulatory Operations Specialist. Regulatory Operations Specialist. ...
The Corporate Information Services Department is seeking a dynamic and talented Senior Clinical Informatics Specialist. The Senior Clinical Informatics Specialist provides guidance in identifying, developing, implementing, and maintaining an efficient and effective clinical information system. ...
The Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Pasted"><strong><u>Regulatory Affairs Specialist </u></strong></p><p><em>Z...