Coordinate the day-to-day administrative activities of the clinical research trials program, including mentoring Research Regulatory Specialists with a focus on study activation. Lead a team of Research Regulatory Specialists and/pr Coordinators. Prepare and/or provide guidance to Regulatory Special...
A company is looking for a Regulatory Change and Research Specialist. ...
The Regulatory Affairs Specialist will be the regulatory representative on product development teams and will be responsible for developing regulatory strategies, authoring submissions, and assessing design and manufacturing changes for wide range implantable products. Works with regulatory and cros...
A company is looking for a Senior Regulatory Affairs Specialist, Medical Devices. ...
Monitors the overall compliance program at the operating level and works closely with the Quality & Regulatory Manager. Tracks and maintains records as per regulatory requirements. Brings potential diversion activities and security breaches to the attention of the Compliance Coordinator or the Regul...
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...
They are responsible for coordinating regulatory filings, communicating regulatory permitting requirements and updates from agencies, and working collaboratively and cross functionally both internally within operations team and with outside parties, including state and federal agencies, continually ...
The Regulatory Affairs Specialist will be the regulatory representative on product development teams and will be responsible for developing regulatory strategies, authoring submissions, and assessing design and manufacturing changes for wide range implantable products. Works with regulatory and cros...
As a Regulatory & Scientific Affairs Specialist, you will provide tactical regulatory expertise to help bring Innovation and Renovation projects to the market through cross collaboration with Marketing, Purchasing, Quality and R&D. Regulatory & Scientific Affairs Specialist. Serve as regulatory repr...
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...
As a Quality Specialist IV in Regulatory & Event Operations (REO), you will review the completed work from the different areas within REO against policies and procedures. Join the team that supports the Regulatory & Event Operations to do the right thing for our customers. If you are detail-oriented...
Monitors the overall compliance program at the operating level and works closely with the Quality & Regulatory Manager. Tracks and maintains records as per regulatory requirements. Brings potential diversion activities and security breaches to the attention of the Compliance Coordinator or the Regul...
Monitor emerging regulatory policy issues, including issues arising from North American regulatory authorities, legislatures, within the pharmaceutical industry or elsewhere, and identify those issues likely to impact Client R&D pipeline, regulatory strategy or product portfolio. Accountable for sup...
The Regulatory Affairs Specialist is responsible for supporting the development and implementation of the overall objectives and regulatory strategies that impact the introduction of new products, and the market status of existing products. The Regulatory Affairs Specialist I will assist Regulatory ...
Regulatory Affairs Specialist. The regulatory Affairs specialist works to provide centralized support within the Office of Clinical Research (OCR) to multiple Principal Investigators (PIs) across the College and its affiliates. Maintains study regulatory database, OCR regulatory database as applicab...
Provide strategic direction and environmental support to Chevron pipeline operations and projects in East Texas, including supporting environmental regulatory permitting, compliance, waste and water management, and regulatory and corporate reporting. Engage externally with third-party consultants an...
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...
Senior Regulatory Affairs Specialist. Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. Work with Regulatory and CFT to improve efficiency in regulatory deliverables. Understand, investigate and evaluate regulatory history/backg...
The Regulatory Compliance Specialist will partner with the Regulatory Compliance Managers to submit and process licenses, permits, Sara Title II, CA CERS and other regulatory reporting. This role will be a strategic partner by working closely with branch operational staff to ensure compliance with a...
As a Project Regulatory Specialist, you will be at the forefront of ensuring that our transmission projects meet all environmental and regulatory requirements. Project Regulatory Specialist RC24-02. Join Our Team as a Project Regulatory Specialist!. Brazos Electric Power Cooperative is seeking a ded...
Regulatory Affairs Specialist provides regulatory guidance, monitoring and administrative help to the Institutional Review Board, Institutional Animal Care and Use Committee and Data and Safety Monitoring Board and other people involved in the conduct of research at all Baylor Scott & White Health. ...
Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. Compile and maintain regulatory documentation databases or systems. Coordinate efforts associated with th...
Develop strategies for worldwide product registration with global regulatory agencies. Author and prepare regulatory submissions for new products and changes. Review significant regulatory issues with supervisors and resolve submission issues. Develop regulatory strategies and provide ongoing suppor...
Responsible for filling necessary registrations with and emphasis on the western hemisphere regulatory entities for all chemical products. Assisting and updating procedures to ensure regulatory compliance. Maintaining documentation to ensure regulatory compliance. ...
Support the IVDR project by revising the assigned technical files.Each technical file must be generated using the latest technical file template and it must clearly present the product, its characteristics and its expected performance to easily and fully understand the evidence of conformity.Each te...