Medical Device Jobs - Remote Work From Home & Flexible
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Featured10 days ago带领新客户的质量倡议,引擎ering and development, first article and sustaining production. Lead and document customer complaint investigations with cross functional teams, suppliers, manufacturing, engineering, program managers.
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1 week agoResponsible for leading a team of engineers in the creation of new product features and enhancing existing features, for our suite of Android-based embeddeddevices. This includes distilling product features down to requirements, guiding the implement...
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25 days agoDesign, develop, and deploy new features for the company's camera systems in in a secure, privacy preserving way. Coordinate across teams on a breadth of platforms including desktop, mobile applications, and backend services. Participate in technical...
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30+ days agoMedicalTranslators needed for a remote freelance position. Translate and edit content from English into Irish (Ireland) with original meaning conveyed in a manner that is readable and understandable to target audience. Minimum 3 years' experience.
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New!3 days agoAct as a leadmedicalwriter on several projects from simple to complex level. Produce clinical documents as required. Provide scientific andmedicalwriting consultancy to clients and internal colleagues at a moderate level. Lead project teams...
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30+ days agoAct as a leadmedicalwriter on several projects from simple to complex level. Produce clinical documents as required. Provide scientific andmedicalwriting consultancy to clients and internal colleagues at a moderate level. Lead project teams in...
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30+ days agoTake responsibility for a feature or module and deliver with high quality. Be responsible for a certain amount of QA/quality of your work. Write automatable code. Document work, test cases, and interact with program, product, QA, and other engineers.
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25 days agoOrganize and participate in variousmedicaleducation events, such as fairs, workshops, cadaverlabs, and live surgery broadcasts, to provide physicians and healthcare professionals with a high-quality educational experience. Work collaboratively...
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30+ days agoWrite and edit clinical development documents. Critically evaluate, analyze, and interpret themedicalfo文献选择的主要资源材料r adequate study design. At least 3 years of previous experience in the pharmaceutical industry.
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Featured9 days agoHelpingmedicalprofessionals work Anywhere. Lowering your carbon footprint by commuting less. Modeling a healthy work-life balance. Knowledgeable about basicmedicalterminology, and have either formal education or experience in themedicalfield.
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30+ days agoWrite IND modules, NDA modules & other related regulatory documents. Write clinical study reports, protocols, and protocol amendments. Coordinate quality control reviews of documents and maintain audit trails of changes. Interact closely with sponsor.
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30+ days agoThis person will use the PICOTS analytic framework to analyze published studies, assess strength of evidence (using the GRADE-based system), and write rapid and in-depth evidence assessments for clinical evidence assessment membership services.
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23 days agoDevelop and execute marketing strategies and campaigns targeting enterprise-level customers, driving alignment with, and execution of, company objectives and achievement of revenue growth goals. 5+ years of experience in B2B product/solution or...
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30+ days agoSet project timelines, budget, necessary procedures, staffing requirements and resources in various phases of IVD projects. Must have a bachelor's degree, 4 years of PM experience, and 2 years inmedical devicetrials. Remote with as-needed travel.
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30+ days agoDrive material compliance to applicable global product and/or packaging regulatory/environmental legislations (e.g. California Prop 65, RoHS, Conflict Minerals, EUMedical DeviceRegulation) for product portfolios. With minimal support, develop...
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Featured12 days agoTo conceptualize, prototype, design and bring newmedical devicesfrom inception through manufacturing and launch following a formal and regulatedmedical devicedesign control process. Responsible for the life cycle ofmedical devicesfrom initiation...
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22天前You'll be supporting venture-backed healthcare startups in the biotech,medical device, or telehealth sector. Work on a variety of tasks, from facilitating client meetings to reconciling accounts, and everything in between. No two days will be the same.
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30+ days agoThis position contributes to chemical characterization study design formedical deviceand pharmaceutical products, justification and defense of laboratory studies to global regulatory agencies,medical devicebiological evaluation plan and risk...
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24 days agoThe CRM in close collaboration with senior clinical research staff and faculty investigators, is responsible for managing significant aspects of up to 5 - 15 different Vascular and Cardiothoracic Surgery Research clinical anddevicetrials.
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30+ days agoConducting a comparison of data recorded on Case Report Forms against source documents, verifying Informed Consent Forms (ICFs) for accuracy and completeness, reviewing regulatory documents anddeviceaccountability records. Ensuring clear...
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FeaturedNew!5 days agoIdentify information sources and resources for local, regional and global regulations. Collect and organize information on regulatory requirements for in vitro diagnosticdevices, quality, preclinical and clinical data to meet applicable regulations.
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30+ days agoResponsible for providing real-time response for the wirelessly enabled monitoringdeviceon a 24/7/365 basis. Additionally, coaching and education are to drive behavior changes that positively impact clinical outcomes and overall health status within...
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! You will collaborate, remotely and asynchronously, with primary care providers nationwide and across care...
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Engage with providers eager to have access to specialty care impact the patients that need it most...
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Engage with providers eager to have access to specialty care. Impact the patients that need it most.
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Engage with providers eager to have access to specialty care impact the patients that need it most.
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Engage with providers eager to have access to specialty care impact the patients that need it most.
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30+ days agoWe are committed to bringing a diverse and inclusive team together focused on solving specialized healthcare. Respond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone!
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Ensure that the specialist feels connected by holding quarterly meetings, provide monthly progress reports.
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Our mission is to foster informed, effective, and trusted care delivery for all patients by every provider.
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30+ days agoOrthopedics Telehealth Physician needed for a remote position. Respond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Have minimum 3 years of practice experience.
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15 days agoWork with scientists,medicalleads, biostatisticians and the clinical affairs team to plan write and edit clinical study protocols and CSRs for registrational studies. Work efficiently and accurately adhering to best practices and departmental...
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30+ days agoRespond to consult requests within 24 hours, Monday through Friday you can respond from anydevicewith internet access; even your phone! Average earning potential is $20,000/annually. Supplement your income. Engage with providers eager to have access.
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30+ days agoAs the Senior Quality Manager you will support the team, working to specify and implement a QMS solution that meets IVDdevicedevelopment requirements in-house and externally with our partners. You will act cross functionally between internal...
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New!3 days agoLead, facilitate, coordinate, and track day-to-day activities required to ensuremedical deviceimplementation projects are completed on time, successfully, and in a manner consistent with organizational goals, departmental policies, established...
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30+ days agoUnder minimal supervision, theMedicalWriter will critically evaluate, analyze, and interpret themedicalfo文献选择的主要资源材料r adequate study design, statistical significance, scientific rigor and absence of bias.
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18 days agoPerform an initial evaluation of the referral appropriateness for company services. Review for information needed to make amedicalnecessity determination. Request additional clinical information when needed to render a decision and determine next...
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Featured23 days agoAssists the Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g, adjudication support,medicalmonitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management.
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30+ days agoResponsible for scientific and strategic relationships with customer stakeholders at priority accounts. The Senior Value Evidence Liaison works closely with Market Access andMedicalAffairs colleagues to ensure that key value evidence is conveyed to...
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New!YesterdayThe Centralized Collections Office (CCO) Specialist - Remote ensuresmedicalcollections for services provided is accurate, timely and fully documented, from a Centralized Collections Office. Provide efficient cash collection through excellent...
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30+ days agoPsychiatrist to join our growing team to improve access to and delivery of healthcare across the nation.MedicalAssociates works in tandem with company to deliver specialty guidance and recommendations through video consults with primary care...
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New!5 days agoProvide supervision & leadership to global team of Complaint Specialists. Manage & balance assignment of work to team to meet goals. Provide guidance, performance feedback & opportunities for growth through regular one-one-one and team meetings.
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30+ days agoSite selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out. Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned...
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28 days agoPerform verification of benefits to determine coverage and payer requirements. Load all benefit information correctly to allow for clean claims and streamlined revenue. Interview patient/caregiver to gather, confirm, and inputmedical, insurance and...
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30+ days agoThe Senior Value Evidence Liaison position is responsible for scientific and strategic relationships with customer stakeholders at priority accounts. The Senior Value Evidence Liaison works closely with Market Access andMedicalAffairs colleagues to...
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16 days agoPerform an initial evaluation of the referral appropriateness for services. Review for information needed to make amedicalnecessity determination. Request additional clinical information when needed to render a decision and determine next steps.
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Featured24 days agoProvides scientific leadership to patient preference team members. Maintains line of research and expertise in relevant scientific areas, along with connections with new literature and regulatory documents. Publishes scientific work in journals...
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30+ days agoPerform all type of visits from site feasibility to close out visits according to plan, document actions and follow up on action plans. Train and guide site staff in safety information handling, systems, protocol and trial procedures to minimize ...
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30+ days agoCandidate will perform the billing and collection activities necessary to facilitate the payment for the services provided and functions as an advocate for and a resource to clinic administration in the areas of reimbursement and managed care.
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8 days agoAs a resident Regulatory Affairs Manager specifically focusing on FDA, you will serve as a key advisor and strategic consultant, assisting with FDA clinical trial filings, answering FDA's questions, and providing strategies on product registration and...
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