Senior Regulatory Affairs Specialist working independently, is responsible for fulfilling regulatory compliance requirements by applying an understanding of regulatory standards and regulations for medical devices, pharmaceuticals, or biologics. As a Senior Regulatory Affairs Specialist you play a p...
A company is looking for a Principal Regulatory Affairs Specialist, US Regulatory Policy. FDA regulatory requirements and policyRegulatory experience within the medical device industry or a regulatory agencyExperience in advocacy related to healthcare policy and regulationsStrong research and analyt...
We are actively seeking a highly skilled Principal Regulatory Affairs Specialist to lead our FDA, Health Canada, and/or EU MDR submissions process. Maintains proficiency in worldwide regulatory requirements; monitors changes in the regulatory landscape and is responsible to communicate these changes...
A company is looking for a Regulatory Change and Research Specialist. ...
Director/Principal Specialist, Regulatory Affairs - Permanent - Denver, CO. Proclinical is seeking a Director/Principal Specialist, Regulatory Affairs for a rapidly growing and exciting medical technology company specializing in SaMD with AI/ML with their location in the Denver, CO area. The Directo...
A company is looking for a Regulatory Affairs Specialist responsible for managing regulatory activities related to the Lung Health product portfolio. ...
The Regulatory Specialist will be responsible for ensuring that the claims made for our dietary supplement products are substantiated by scientific evidence and comply with regulatory requirements. We are looking for a positive, driven, and detail-oriented Regulatory Specialist to join our growing t...
The Regulatory Specialist will be responsible for ensuring that the claims made for our dietary supplement products are substantiated by scientific evidence and comply with regulatory requirements. We are looking for a positive, driven, and detail-oriented Regulatory Specialist to join our growing t...
As part of the continued growth and innovation of our Capital Project Delivery service offering, ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm as a Principal Biologist/Regulatory Specialist, Power and Renewables. This Principal ...
ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm as a . Principal Biologist/Regulatory Specialist. Principal Biologist/Regulatory Specialist. Serve as Project Biologist/Regulatory Specialist for environmental impact assessment unde...
Senior Regulatory Affairs Specialist responsibilities include, but are not limited to, the following:. Under the direction of the Manager, Regulatory Affairs and Quality Assurance, this position in tandem with Senior Management, will assist with ensuring that DPT's laboratories are compliant with th...
Training on the relevant regulatory requirements can be provided for exceptional candidates with an interest in Regulatory reporting, who can demonstrate excellent performance in their current and previous roles. The Regulatory Reporting function has recently been aligned to Investment Operations wi...
Regulatory & Compliance Specialist. Regulatory & Compliance Specialist in our Raleigh, NC or Denver, CO locations. Responsible for working with Project Managers and project teams to ensure successful project execution and delivery of telecommunications regulatory documents, reviews, and permitting. ...
Senior Regulatory Affairs Specialist responsibilities include, but are not limited to, the following:. Under the direction of the Manager, Regulatory Affairs and Quality Assurance, this position in tandem with Senior Management, will assist with ensuring that DPT’s laboratories are compliant with th...
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...
Under the direction of the Manager, Regulatory Affairs and Quality Assurance, this position in tandem with Senior Management, will assist with ensuring that DPT’s laboratories are compliant with the regulatory and accrediting organizations that oversee our laboratories. The Regulatory Affairs Specia...
Clinical Research Regulatory Specialist. The primary focus is on the development, submission, maintenance, filing and reporting of regulatory documents while achieving and maintaining compliance with all internal, external and federal policies and regulations that apply to research involving human s...
Senior Regulatory Affairs Specialist responsibilities include, but are not limited to, the following:. Under the direction of the Manager, Regulatory Affairs and Quality Assurance, this position in tandem with Senior Management, will assist with ensuring that DPT's laboratories are compliant with th...
Reporting jointly to the Faculty Support Manager and the Executive Associate Dean of Academic Affairs, the Faculty Support and Compliance Specialist will (1) collaborate with other members of the Faculty Support Team to provide high-level administrative support to faculty members in the realms of te...
You will also be responsible for establishing, monitoring and providing oversight or acting as a liaison for compliance programs, processes and department of insurance examinations, as well as making recommendations to leadership on compliance matters that affect the product portfolio, forms, system...
Job Title: Business Services Program Manager. The Colorado Area Health Education Center (AHEC) Program Office works to build state-wile network capacity and strengthen academic-community linkages in four core mission areas: health careers and workforce diversity; health professions student education...
Under direction of the Program Director of Clinical Trials Operations, the Program Manager will be responsible for the planning, development, management, and implementation of the Clinical Research Recruitment Program in the Office of Clinical Research Operations and Services (CROS). Assist with oth...
The Compliance Analyst is responsible for the successful compliance management and delivery of compliance services for a block of business. You'll develop a strong knowledge of regulation requirements for compliance services and participate in training and communication of compliance administration ...
A company is looking for a Manager, Materials (Program Development). ...
A company is looking for a Senior Technical Project Manager, Platform Engineering in New York, NY or Remote (USA). Key Responsibilities:Build a complete understanding of the ongoing developments to the Avalanche protocol and communicate it to downstream teamsKeep stakeholders informed on dependencie...