If you’re up to the challenge, then take a chance at this rewarding opportunity! Position Overview: Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence – JD Th...
read moreIf you’re up to the challenge, then take a chance at this rewarding opportunity! Position Overview: Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence – JD Th...
read moreKey ResponsibilitiesTrack new and pending state legislative and regulatory proposals affecting the CPA professionConduct policy research and assist in drafting advocacy materialsProvide administrative...
read moreKey ResponsibilitiesTrack new and pending state legislative and regulatory proposals affecting the CPA professionConduct policy research and assist in drafting advocacy materialsProvide administrative...
read moreOur client, a major bank in New York City, is looking for talented Technology Regulatory Affairs Specialist. We are seeking a dynamic and detail-oriented Technology Regulatory Affairs Specialist. Tech...
read moreOur client, a major bank in New York City, is looking for talented Technology Regulatory Affairs Specialist. We are seeking a dynamic and detail-oriented Technology Regulatory Affairs Specialist. Tech...
read moreKey ResponsibilitiesContribute to regulatory plans and assessments to meet various regulatory requirementsPrepare regulatory submissions and provide guidance on strategy and requirementsSupport compli...
read moreKey ResponsibilitiesContribute to regulatory plans and assessments to meet various regulatory requirementsPrepare regulatory submissions and provide guidance on strategy and requirementsSupport compli...
read moreKey ResponsibilitiesContribute to regulatory plans and assessments to meet various regulatory requirementsPrepare regulatory submissions and provide guidance on strategy and requirementsSupport compli...
read moreKey ResponsibilitiesContribute to regulatory plans and assessments to meet various regulatory requirementsPrepare regulatory submissions and provide guidance on strategy and requirementsSupport compli...
read moreOur Senior Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing product portfolio, in addition to opportunities to provide regulatory supp...
read moreOur Senior Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing product portfolio, in addition to opportunities to provide regulatory supp...
read moreRegulatory Affairs Project management experience. Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects a...
read moreIntegration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...
read moreThe PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...
read moreThe Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...
read moreThe Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...
read moreThe Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...
read moreThe Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...
read moreMust have experience working on regulatory items for research protocols. Performs quality control, research source documentation verification against case report form data, including informing the sit...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities. ...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Anticipate regulatory obstacles and emerging issues throughout the product submission. Monitor and submit applic...
read moreProvides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of client's products and processes. Knowledge in relevant Regulatory Affairs areas...
read moreThis position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...
read moreThis position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...
read moreEligibilities & qualifications.
Working knowledge of relevant federal and state regulatory programs (e.
Working knowledge of relevant federal and state regulatory programs (e.
The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...
read morePrepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both dom...
read moreRegulatory Affairs Specialist Project Lead I (Scientific). At least - years of relevant pharmaceutical/biotechnology experience in R&D, including at least years of relevant Regulatory Affairs experien...
read moreRegulatory Affairs Specialist Project Lead I (Scientific). At least - years of relevant pharmaceutical/biotechnology experience in R&D, including at least years of relevant Regulatory Affairs experien...
read moreRegulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...
read moreRegulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...
read moreSupport Distribution Center management and designated staff on the actions necessary to maintain regulatory compliance. Provide guidance to the company and subsidiaries to perform actions in order to ...
read moreThis role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Stra...
read moreThis role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Stra...
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