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We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management and compliance activities for pharmaceutical or medical device products. · 2–5+ years of Regulatory Affairs experience (Pharma Biotech or Medical Devices) · Strong knowledge of F ...
Raleigh, NC2 weeks ago
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We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management compliance activities for pharmaceutical medical device products. · This is a W2 contract role supporting ongoing regulatory operations in a fast-paced GxP environment. · Prepare ...
Raleigh2 weeks ago
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This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function. · ...
Raleigh3 days ago
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This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function. The position focuses on processing and tracking contracts, purchase requests, purchase orders, and invoices. · The role is well suit ...
Raleigh, NC1 week ago
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This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function.The position focuses on processing and tracking contracts, purchase requests, purchase orders, and invoices. · ...
Raleigh1 week ago
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This position will independently manage essential regulatory documentation for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies. The Regulatory Affairs Specialist will interact ...
Raleigh, NC1 week ago
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Independently manage essential regulatory documentation for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Assist/Advise project ...
Raleigh1 week ago
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The Regulatory Affairs Specialist will be responsible for a wide variety of regulatory activities for sustaining products including medical devices and Software as Medical Device (SaMD) and regulatory operation. · ...
Morrisville3 weeks ago
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The Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development, design changes, and field safety corrections, · Author EU MDR technical files and will contribute to other international regulatory submissions. · Particip ...
Creedmoor Full time1 month ago
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The Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development, design changes, and field safety corrections, · Author EU MDR technical files and will contribute to other international regulatory submissions. · Particip ...
Creedmoor, NC, US1 day ago
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Job summaryThe Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development... · ...
Creedmoor, NC4 weeks ago
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Perform assessment of CMC changes, identifying global regulatory requirements. · ...
Durham1 month ago
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Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...
Morrisville1 month ago
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Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...
Morrisville, NC1 month ago
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Developing global regulatory submissions for medical device industry with EU MDR experience required. · ...
Durham2 weeks ago
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Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...
Durham Full time1 month ago
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++This position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory approval. · +++Prepares robust regulatory applications to achieve departmental and organizational objectives. · Creats reviews and ...
Durham1 month ago
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· The Specialist supports the coordination and delivery of public affairs, stakeholder engagement, community relations, and communications activities across Carnival Corporation's global destination portfolio. · This role requires addressing complex operational challenges in a d ...
Bahama, NC2 weeks ago
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The Division of Academic & Student Affairs (DASA) is where students discover connections and community. It is where students live, where they gather, where they improve themselves, each other, · & their university. DASA serves all students at NC State through three integrated com ...
Raleigh, NC2 weeks ago
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This position will provide information and guidance to students and others regarding the VA Educational benefits process while ensuring compliance with the Department of Veterans Affairs (DVA). · The individual in this position will also perform specialized tasks that only VA app ...
Raleigh, NC1 week ago
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The North Carolina Department of Administration is seeking applicants for a Raleigh based Program Analyst II (Working Title: Deputy Director) for the Commission of Indian Affairs Division (CIA) to assist and help lead the Division operations in meeting its legislative mandate as ...
Wake County, NC $64,621 - $88,695 (USD) Full time3 weeks ago
Regulatory Affairs Specialist - Raleigh, NC - beBeeParalegal
Job title: Regulatory Paralegal : 200318
Description
Job Description
We are seeking a detail-oriented individual to support legal and regulatory proceedings in a deadline-driven environment. The successful candidate will be responsible for document preparation, quality control, docket tracking, and coordination with internal teams, outside counsel, and regulatory agencies.
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Regulatory Affairs Specialist
Only for registered members Raleigh, NC
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Regulatory Affairs Specialist
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Medical Affairs Admin/Project Specialist
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Medical Affairs Admin/Project Specialist
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Medical Affairs Admin/Project Specialist
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Senior Regulatory Affairs study Start Up Specialist
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Senior Regulatory Affairs study Start Up Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Sr. Regulatory Affairs Specialist
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Sr. Regulatory Affairs Specialist
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Sr. Regulatory Affairs Specialist
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Sr. Regulatory Affairs Specialist
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