Medical Writer IV - Regulatory CERs (Remote)
Abbott
New York, NY
- Remote job
Abbott is seeking a Medical Writer IV to support Regulatory Clinical Evaluation for vascular medical devices. This role involves developing and maintaining Clinical Evaluation Reports (CERs) and related regulatory documentation across the product lifecycle. The ideal candidate has extensive medical writing experience in medical devices or related fields, with strong collaboration across Regulatory Affairs, Clinical Affairs, Quality Engineering, R&D, and Medical Affairs to ensure compliant #J-18808-Ljbffr Abbott
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Medical Writer IV - Regulatory CERs (Remote) in New York, NY vacancy
- ManpowerGroup’s Experis is seeking a Medical Writer IV to support the Regulatory Clinical Evaluation team for vascular medical devices. On-site positions... ...cross-functional collaboration skills. You will author CERs/CEP, CER plans, and related documents while ensuring ISO...Regulatory
- A global medical device consulting firm is looking for a EUMDR Medical Writer for a remote, full-time engagement. Candidates should have a minimum of 5 years of medical or... ..., literature reviews, and compliance with regulatory guidelines. Strong written and oral communication...Remote jobRegulatoryFull time
$65 - $68 per hour
Akkodis is seeking a Medical Writer IV for a 12-month contract with remote/on-site options, including Plano, TX. Compensation is $65-68 per... .... The Medical Writer will support the regulatory clinical evaluation team, craft CER documents, and contribute throughout the product...Remote workRegulatoryHourly payContract work$66 - $71 per hour
Our client is seeking a Medical Writer IV to join their Regulatory Clinical Evaluation team. As a Medical Writer IV... ...locations, with the possibility of fully remote for qualified candidates who are... ...to plan for and support CER-related projects, processes, and deliverables...Remote workRegulatoryPermanent employmentFor contractorsWork experience placement$65 - $68 per hour
Akkodis is seeking a Medical Writer IV for a 12-month contract with a client for Remote/ Onsite. Title: Medical Writer IV Location... ...Evaluation Reporting / Medical Writer (CER) for Vascular Medical Devices The Medical Writer on our Regulatory Clinical Evaluation team...Remote workRegulatoryFull timeContract workTemporary workWork experience placementLocal area- ...Make an Impact as a Medical Writer II at Worldwide Bring your medical... ...communication help support Phase I-IV clinical studies across the... ...high-quality clinical and regulatory documents that contribute to... ...Where You'll Work This is a REMOTE role open to candidates based...Remote workRegulatoryWork at officeWorldwideNight shift
Worldwide Clinical Trials
United States13 hours ago $78k - $156k
...businesses and products in diagnostics, medical devices, nutritionals and... ...for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides... ...in planning for and supporting CER related projects and processes....RegulatoryWork experience placementWorldwideShift workAbbott
Maple Grove, MN2 days ago- ...all phases, offering Phase I-IV and real-world studies. With... ...Emerald Clinical has helped drive medical breakthroughs through deep... ...clinical plan outlines, sections of regulatory submission documents, and... ...Flexibility: Enjoy hybrid or remote working arrangements, depending...Remote workRegulatoryLocal areaWorldwide
Emerald Clinical Trials
United States5 days ago - ...deep domain expertise in regulatory sciences, clinical... ...compliance, pharmacovigilance, medical information, and R&D... ..., IBs, ICFs, CEPs/CERs, DSURs, and plain language... ...less experienced medical writers, as necessary. ~... ...ProPharma supports remote working, we also recognise...Remote workRegulatoryContract workWork at office
ProPharma Group
Western Springs, IL4 days ago $90k - $140k
...Senior Medical Writer Everest Clinical Research ("Everest") is a full... ...Canada on-site location, or remotely from a home-based office anywhere... ...documents supporting regulatory submissions for clinical trial... ...therapeutic areas and Phase I through IV clinical trials an asset (...Remote workRegulatoryContract workTemporary workWork from homeWorldwideEverest Clinical Research
United States5 days ago- ...Clinical FSP is currently seeking a EUMDR Medical Writer for a remote long term engagement with one of our... ...the medical device industry and CER document creation under MEDDEV 2.7/1... ...development, risk management, quality regulatory compliance, adverse event reporting....Remote workRegulatoryFull timeWork at office
Kelly Science, Engineering, Technology & Telecom
New York, NY4 days ago - Clin Evaluation Med Writer Job Location: Virtual, MN Duration: 12... ...The Senior Clinical Evaluation Medical Writer is responsible for... ...and reports in compliance with regulatory requirements and industry standards... ...clinical evaluation reports (CERs) and related documents....Remote jobRegulatoryShift workDay shift
- ManpowerGroup’s client, a leader in medical device innovation, seeks a Medical Writer IV to join the Regulatory Clinical Evaluation team in Santa Clara, CA. The role focuses on authoring Clinical Evaluation Plans/Reports and related documents across the product life cycle...Regulatory
- Get notified about new Medical Writer jobs in United States . 6,000+ Medical Writer Jobs in United States Senior Medical... ...Senior Medical Writer - Clinical Evaluation Reporting (CER) Principal Medical Writer, Regulatory & Scientific Writing Senior Regulatory Medical Writer...RegulatoryWork at office
$65k - $100k
Job Title: Medical Writer Type of company: Full-service Clinical Research... ...bonus opportunity Location: Remote anywhere in Canada, US or UK... ...This role combines clinical and regulatory writing with document quality... ...areas and Phase I-IV clinical trials. A good understanding...Remote workRegulatoryWork at office$67 per hour
...reached on # . We have Contract role Medical Writer f or client at Santa Clara CA. Please let... ...Evaluation Reporting / Medical Writer (CER) for Vascular Medical Devices The Medical Writer on our Regulatory Clinical Evaluation team provides technical and...RegulatoryHourly payPermanent employmentContract workWork experience placementShift workgeneris Tek
Green Oaks, IL6 days ago$90k - $140k
Job Title: Senior Medical Writer Type of company: Full-service Clinical... ...performance-based bonus Location: Remote within the US, or Canada. UK... .... You’ll lead clinical and regulatory writing projects from initial... ...areas and Phase I-IV clinical trials. A strong understanding...Remote workRegulatoryWork at office- ...Job Description Senior Medical Writer - Clinical Development \n \n Immix Biopharma, Inc. \n \n United States / Remote / LA, CA \n \n Our 3 Core Values \n \n... ...for preparing, reviewing, and editing regulatory documents required for submission to the...Remote workRegulatoryOdd job
Immix Biopharma (Nasdaq: IMMX)
West Virginia10 days ago - ...Scientific community. We are currently looking for a REMOTE Associate Director Medical Writer to work for a leading San Diego biotech company. Responsibilities... ...with Clinical Development, Biostatistics, and Regulatory teams to translate complex data into clear, high-...Remote workRegulatoryWork at office
BioPhase
United States1 day ago - ...Overview Revelation Biosciences is seeking a mid-level Regulatory Medical Writer to develop high-quality clinical and regulatory documents supporting... ...well-structured, and submission-ready documents. This is a remote-friendly position open to candidates able to collaborate...Remote workRegulatoryFull time
Revelation Biosciences Inc.
San Diego, CA2 days ago $128k - $160k
...Principal Medical Writer, Regulatory & Scientific Writing Location: Remote or Hybrid in San Diego Employment Type: Full time Reports To: President & Founder About Aroga Aroga Biosciences is a full-service CRO providing expert medical writing, regulatory...Remote workRegulatoryFull timeAroga Biosciences
San Diego, CA4 days ago- ...Freelance Medical Writer Pharmaceutical / Medical Communications Projects Logan Elite is... ...references Familiarity with Medical/Legal/Regulatory (MLR) review Experience in one or... ...Details Freelance / Contract Remote Project-based and longer-term opportunities...Remote workRegulatoryHourly payContract workFreelanceFlexible hours
Logan Elite
United States4 days ago $75k - $120k
...Digital Producer / Medical Writer SurvivorNet, New York, primarily on-site Base salary:... ...go through client medical, legal, and regulatory review. What we’re looking for We... ...our headquarters in New York City. Some remote work is possible, but you should expect...Remote workRegulatoryWork at officeSurvivorNet
New York, NY3 days ago- ...Job Title Provides high-quality regulatory medical and scientific writing in support of Phase 1–3 clinical development of pharmaceutical... ...Application (MAA) documents. Reviews documents prepared by junior writers and peers. May provide training and mentorship to junior...Remote workRegulatoryContract work
Katalyst HealthCares & Life Sciences
United States2 days ago $150 per hour
...Base pay range $150.00/hr - $150.00/hr Medical Writer Contractor-CNS (Home-based) Job Duties: Develop high-quality clinical and regulatory documents: protocols, IBs, CSRs, Module... ...Senior Medical Writer - Contract to Hire REMOTE - Medical/Clinical Reimbursement Policy...Remote workRegulatoryContract workPart timeFor contractorsFreelanceWork from homeHydrogen Group
New York, NY6 days ago- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret...Remote workRegulatoryWorldwide
MMS
Bridgeport, CT4 days ago $95k - $125k
...Senior Medical Writer, Medical Communications Remote, United States Are you passionate about transforming complex science into meaningful, impactful... ...strong domain knowledge across therapeutic areas, regulatory standards, and key statistical concepts You are an...Remote workRegulatoryPrecision AQ
United States2 days ago- ...Medical Writer At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. Through... ...analysis plans and other clinical study documentation that supports regulatory submissions and critical development decisions. This is an...Remote workRegulatoryWork at officeWorldwideFlexible hours
Clario, Inc.
United States5 days ago - ...Medical Writer Join Us as a Medical Writer - Make an Impact at the Forefront of InnovationThe Medical Writer provides high-quality medical... ...oral and written communication skills Good knowledge of regulatory documentation and drug development process Great judgment...Remote workRegulatoryWork at office
Thermo Fisher
United States1 day ago $80.6k - $175.7k
Principal Medical Writer - Publications Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate... ...for scientific meetings. • Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines,...Remote workRegulatoryContract workFlexible hoursSyneos Health Careers
United States1 day ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Writer IV - Regulatory CERs (Remote). Be the first to apply!
Related searches
- medical writer remote New York, NY
- freelance medical writer New York, NY
- medical writer New York, NY
- freelance medical copywriter New York, NY
- senior medical writer New York, NY
- medical editor New York, NY
- medical customer service representative New York, NY
- medical and health service manager New York, NY
- medical driver New York, NY
- non emergency medical transportation New York, NY