Clinical Affairs Program Manager
4 weeks ago
RESPONSIBILITIESCreate and manage detailed project schedule, timelines and project tracking tools for Clinical Evaluation, PMS and Post Market Clinical Follow-up (PMCF) processes for all medical devices and IVDs.Ensure, in conjunction with R&D and other personnel, that the clinical requirements of the product are adequately addressedManage relationship with CROs, as applicable
EXPERIENCEA minimum of 4 years of combined experience in clinical research, medical writing, clinical science in the medical device and/or pharmaceutical industry.Master's degree or Ph.D. preferred.Experience/knowledge in writing CERs and/or PMS plans in accordance with Meddev 2.12.2 and MDR
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Clinical Affairs Program Manager
4 weeks ago
Irvine, United States JCW Full timeApply for an exciting opportunity to join a global Medical Device company. You will be writing many CERs for existing products in line with EU MDR guidelines and contribute to the clinical strategy for new products.RESPONSIBILITIESCreate and manage detailed project schedule, timelines and project tracking tools for Clinical Evaluation, PMS and Post Market...
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Senior Specialist, Regulatory Affairs
2 weeks ago
Irvine, United States Orange County Regulatory Affairs Discussion Group (OCRA) Full timeSenior Specialist, Regulatory Affairs, Sustaining Products, THV The Regulatory Affairs Senior Specialist role is an outstanding opportunity to be a part of the Edwards Lifesciences Transcatheter Heart Valve (THV) program, one of the medical device industry’s most groundbreaking technological innovations. Edwards has a strong pipeline in this space and the...
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Clinical Trial Manager
4 days ago
Irvine, United States Provident Research Inc Full time**Clinical Trial Manager - Major Medical Device Corp**We're seeking an experienced Clinical Trial Manager or equivalent with at least 6 years of clinical trial management experience for this terrific role within a major Medical Devices Company. This is a Hybrid role that is divided into work-from-home and work from corp. offices in Irvine, CA. This is a...
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Senior Specialist, Regulatory Affairs, Critical Care
21 hours ago
Irvine, United States Orange County Regulatory Affairs Discussion Group (OCRA) Full timeSenior Specialist, Regulatory Affairs, Critical Care Company: Edwards Lifesciences LLC Position: Req-33420 Location: Irvine, CA Posted: May 13, 2024 Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory...
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Irvine, United States AbbVie, Inc Full timeCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services...
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Irvine, California, United States AbbVie Full timeJob Description Purpose: AbbVie is dedicated to delivering a consistent stream of innovative, safe, and effective quality medicines and products that solve serious health issues and have a remarkable impact on people’s lives. As a quality organization in research & development, R&D Quality Assurance (RDQA) is committed to driving quality excellence...
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Medical Affairs Analyst
4 days ago
Irvine, United States Intellectt Inc Full timeTitle: Medical Affairs AnalystLocation: Irvine, CA (On-Site)Duration: 6+ Months Job Description: This is a unique opportunity to play an important role in the growing Transcatheter Mitral & Tricuspid Therapies (TMTT) Medical Affairs team, providing innovative solutions to transform treatment for patients suffering from mitral and tricuspid heart disease.This...
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Regulatory Affairs Specialist
2 weeks ago
Irvine, United States Cypress HCM Full time· 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry· Working knowledge of FDA, and CE marking requirements for IVD products is a plus· Able to work independently and with others· Able to work with minimal supervision· Excellent computer applications skills· Strong...
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Regulatory Affairs Specialist
2 weeks ago
Irvine, United States Cypress HCM Full time· 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry· Working knowledge of FDA, and CE marking requirements for IVD products is a plus· Able to work independently and with others· Able to work with minimal supervision· Excellent computer applications skills· Strong...
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Regulatory Affairs Specialist
2 weeks ago
Irvine, United States Cypress HCM Full time· 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry· Working knowledge of FDA, and CE marking requirements for IVD products is a plus· Able to work independently and with others· Able to work with minimal supervision· Excellent computer applications skills· Strong...
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Senior Regulatory Affairs Specialist
2 weeks ago
Irvine, United States Infosoft, Inc. Full timeJob Title: Senior Regulatory Affairs SpecialistDuration: 9 monthsLocation: Irvine, CA (Onsite)Shift: 8 am to 5 pm.Our Client is a Global medical device Manufacturer.We are looking for a Senior Regulatory Affairs Specialist to complete and maintain regulatory approvals and clearances of assigned products.Create regulatory submissions (exercising judgment to...
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Senior Regulatory Affairs Specialist
2 weeks ago
Irvine, United States Infosoft, Inc. Full timeJob Title: Senior Regulatory Affairs SpecialistDuration: 9 monthsLocation: Irvine, CA (Onsite)Shift: 8 am to 5 pm.Our Client is a Global medical device Manufacturer.We are looking for a Senior Regulatory Affairs Specialist to complete and maintain regulatory approvals and clearances of assigned products.Create regulatory submissions (exercising judgment to...
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Irvine, California, United States AbbVie Full timeJob Description The Manager, Regulatory Affairs In Vitro Diagnostics and Companion Diagnostics works with internal and external partners to develop and implement global regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives. Supports regulatory objectives for the management of IVD/CDx...
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Manager, Regulatory Affairs
4 weeks ago
Irvine, California, United States Allergan Aesthetics Full timeJob Description Description The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides guidance to Global Regulatory Lead (GRL) and project team. Plans and prepares complex regulatory submission documents primarily for US regulatory filings. Utilizing...
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Clinical Development Specialist
2 weeks ago
Irvine, United States Edwards Lifesciences Corporation Full timeImagine how your ideas and expertise can change a patients life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients lives. As part of our Clinical Affairs t Clinical, Specialist, Development, Product Development, Manufacturing, Healthcare, Patient, Design
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Scientific - Assoc Analyst, Medical Affairs
5 days ago
Irvine, United States TalentBurst, Inc. Full timeTitle: Associate Analyst, Medical Affairs| Job ID: 6869-1Duration: 6 monthsLocation: Irvine, CA 92614 (fully onsite)Job Description: This is a unique opportunity to play an important role in the growing Transcatheter Mitral & Tricuspid Therapies (TMTT) Medical Affairs team, providing innovative solutions to transform treatment for patients suffering from...
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Principal, Statistical Programming
2 days ago
Irvine, United States Edwards Lifesciences Full timeJob Description Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase...
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Senior Regulatory Affairs Specialist
7 days ago
Irvine, United States NeuroVasc Technologies, Inc. Full timeWe are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence through innovation with integrity. Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning...
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Senior Regulatory Affairs Specialist
4 weeks ago
Irvine, United States NeuroVasc Technologies, Inc. Full timeWe are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and...
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Senior Regulatory Affairs Specialist
1 month ago
Irvine, United States NeuroVasc Technologies, Inc. Full timeWe are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and...