Regulatory & Clinical Lead, Medical Devices (Remote)
LivaNova
- Remote job
LivaNova seeks a Regulatory and Clinical Specialist to support clinical evaluation activities, manage regulatory submissions, and collaborate with various teams on deliverables. This role requires experience in writing Clinical Evaluation Plans and Reports (CEP, CER), along with a solid understanding of EU and FDA regulations. The ideal candidate holds a master’s degree in biomedical engineering or equivalent and has at least 5 years of relevant experience. This position is remote, with occasional travel required. #J-18808-Ljbffr LivaNova
$153k - $160k
Kelly Science & Clinical is seeking a Clinical Strategy Lead for a direct-hire role in a medical device client. Remote, with preference for hybrid work in Plano, TX. Pay range $153,... ...lead study concepts, and collaborate with Regulatory Affairs, R&D, and Medical Affairs....Remote jobRegulatoryMedical device$85k - $95k
LivaNova is seeking a Regulatory and Clinical Specialist to support clinical evaluations, prepare regulatory... ...candidate will have experience in medical writing, specifically with Clinical... ...Plans and technical submissions. This remote role is based in the United States,...Remote jobRegulatoryMedical device- ...holidays, and hybrid or remote work options for many jobs... ....OverviewWe are a global medical device company conducting clinical investigations to support... ...highly motivated Senior or Lead Clinical Research... ...protocol, procedures, and regulatory requirements.Lead or contribute...Remote workRegulatoryMedical deviceH1bLocal area
$154.4k - $242.55k
...Director, GCSC Operations Lead is responsible for... ...Associate Director manages Clinical Supply project... ...investigational product regulatory requirements for delivery... ....Experience with Medical Devices a plus.Strong understanding... ...Takeda’s Hybrid and Remote Work policTakeda Compensation...Remote workRegulatoryMedical deviceMinimum wageContract workTemporary workLocal area$113.3k - $226.7k
...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and... ...JOB DESCRIPTION:Field Clinical Lead ManagerWorking at... ...support.This is a remote position and will have... ...initiatives.Ensure adherence to regulatory requirements (FDA, GCP...Remote workRegulatoryMedical deviceWorldwideShift work$61 - $65.21 per hour
Clinical Project Lead II for Life Cycle Management (LCM) in Vision care 4... ...in Vision care Location: Remote Duration: 06 months Pay Range... ...related documents for Medical Device Regulation (MDR) remediation... ...writing, reviewing clinical regulatory documentation. Experience...Remote workRegulatoryMedical deviceContract work$50 - $75 per hour
...Our client, a Fortune 500 Medical Device company, has engaged GForce... ...Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee... ...compliance with applicable regulatory requirements, Good Clinical... ...institution). Term & Start Remote/home-based; Ideally located...Remote workRegulatoryMedical deviceContract workPart timeLocal areaWork from home$17 - $22 per hour
Clinical Site Lead, Pharmaceuticals, Cardiovascular Clinical Site Lead, Pharmaceuticals... ...Our client, a Fortune 500 Medical Device company, has engaged GForce... ...compliance with applicable regulatory requirements, Good Clinical... ...environment. Term & Start Remote/home-based; Must be located...Remote workRegulatoryMedical deviceContract workTemporary workLocal areaWork from homeDay shift$160.6k - $240.8k
...DescriptionGeneral Summary:The Clinical Study Quality Lead (SQL), Associate... ...compliance with regulatory requirements to... ...trials, understand medical terminology, standards... ...experience with medical device manufacture and... ...as: 1. Hybrid: work remotely up to two days per week...Remote workRegulatoryMedical deviceFull timeWork experience placementSummer workWork at officeFlexible hours2 days per week- ...contract opportunity in Madison, Wisconsin. You will lead and manage technical projects in the medical device industry, focusing on project planning, scheduling... ..., and cross-functional collaboration to ensure regulatory compliance. The role requires mentoring teams, maintaining...RegulatoryMedical deviceContract work
$78k - $156k
...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and... ...The Senior Clinical Monitoring Lead (CML)... ...of monitoring plans, regulatory compliance, timely issue... ...United States of America : Remote ADDITIONAL LOCATIONS:...Remote workRegulatoryMedical deviceFull timeWork experience placementLocal areaShift work$90k - $100k
...Sales Manager Location: Remote (United States) Travel: Approximately 60%... ...growth across North America within the medical device packaging sector. This role focuses on... ...understanding of medical device packaging and regulatory requirements . Selling packaging...Remote workRegulatoryMedical deviceFull timeTemporary workNight shift- ...therapeutic assets.This position is entirely remote and open to candidates across the... ...environment. Experience in areas such as CROs, medical devices, healthcare services, or commercial... ...of therapeutic development, regulatory pathways, and commercialization strategies...Remote workRegulatoryMedical device
- ...-oriented and organized, the full-time remote Quality Associate will manage post-market... ...with quality standards in the medical device industry. Key Responsibilities Review... ...'s degree required; Master's degree in Regulatory Affairs, Quality Systems, or a related...Remote workRegulatoryMedical deviceFull timeWork at office
- A medical device company is seeking a Clinical Research Associate to manage and monitor global clinical studies ensuring compliance with regulatory requirements. This remote position aims to support study site management and assists in the development of clinical study...Remote workRegulatoryMedical device
- ...Supporting analyses of medical device degradation, the full-time salaried Medical Device Engineer... ...and technical consultation related to regulatory reviews and product development for implantable medical devices, working 100% remotely. Key responsibilities Support analyses...Remote workRegulatoryMedical deviceFull time
- ...Pfizer is seeking an Audit Lead to design, deliver, and maintain... ...across aseptic/biologics, medical devices, small molecules andsupplier... ...and PharmSci to ensure regulatory alignment and robust audit evidence... ...travel up to 40% and a remote work option. #J-18808-Ljbffr...Remote workRegulatoryMedical device
$2,550 per week
...licensure requirements, regulatory and practice standards... ...to be able to inform clinical teams regarding... ...events, home visits and remote locations. There may be... ...to assure appropriate medical equipment is arranged... ...durable medical equipment/devices based on needs of patient...Remote workRegulatoryMedical deviceFull timeFlexible hoursShift work- BiVACOR in Huntington Beach is seeking a Clinical Operations Manager to lead the operational framework for groundbreaking clinical studies of the... ...sites, requiring meticulous organizational skills and regulatory knowledge. The ideal candidate possesses a Bachelor’s in...RegulatoryMedical device
- A healthcare technology company is seeking a Sr. Regulatory Affairs Specialist in Somerville, Massachusetts, to support the commercialization... ...environment, and strong communication skills. This position is remote and requires some travel. Competitive salary and benefits...Remote workRegulatoryMedical device
- ..., Inc. in Hayward, CA is seeking a Sr. Clinical Trial Manager to oversee global trials... ...CROs, and sites to ensure data quality, regulatory compliance, and timely study deliverables... ...7+ years in clinical research within medical devices, strong ICH GCP knowledge, and experience...RegulatoryMedical device
- ...assist the FDA's Center for Devices and Radiological Health (CDRH) with regulatory responsibilities, including supporting medical device reviews and... ..., all while working 100% remotely. Key responsibilities Support... ...ten years of relevant clinical experience in surgical oncology...Remote workRegulatoryMedical devicePart time
- ...Serving as the regulatory affairs lead on cross-functional teams, the full-time Principal Regulatory... ...across global markets while working remotely in the United States. Key... ...coordinate activities for assigned drug and medical device products Provide regulatory review and...Remote workRegulatoryMedical deviceFull time
- ...support the design and implementation of packaging and labeling solutions for medical device products, the 3-4 month contracted remote Packaging & Labeling Engineer will ensure compliance with regulatory requirements and quality standards while collaborating with cross-...Remote workRegulatoryMedical device
$120k - $140k
...for the brain, from clinical development to... ...partners, we offer the leading at-home EEG... ...business, customer, and regulatory requirements. You... ...be working in the Device Team, reporting to... ...a first-class remote work experience, but... ...and regulations for medical devices. The...Remote workRegulatoryMedical deviceFull timeWork experience placementWork at office3 days per week- ...developing, and maintaining medical devices and technologies that enhance... ...ensuring compliance with regulatory standards. You will collaborate cross-functionally with clinical teams and other engineers to... ...development. This position may be remote with travel as needed by the...Remote workRegulatoryMedical device
- VB Spine, a leading privately held spine company, is seeking a Sr. Staff Regulatory Affairs Specialist to drive global regulatory strategies for complex medical devices. This role partners with cross-functional teams to support development, lifecycle management, and submissions...Remote jobRegulatoryMedical device
- ...Seeking a remote contract Medical Device Quality Engineer, the candidate will lead investigations into electrical failures, conduct root cause analyses, and collaborate... ...actions, ensuring product quality and regulatory compliance over a 6-12 month period. Key responsibilities...Remote workRegulatoryMedical deviceContract work
- ...with pharmaceutical, biotech, and medical device organizations to address complex regulatory and operational challenges. The... ...leadership. Key Responsibilities Lead and deliver client engagements within... ...relationships is preferred Fully remote role Occasional client travel as...Remote workRegulatoryMedical deviceFull time
- A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses... ...scientific information into regulatory-ready documents. Candidates... ...encouraged to apply. This is a remote role with an initial...Remote workRegulatoryMedical deviceContract work
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