Senior Medical Writer, Clinical Evaluation & Regulatory
Abbott
Abbott in Maple Grove, MN is seeking a Senior Medical Writer, Clinical Evaluation to join our Regulatory Clinical Evaluation team. The role provides technical and strategic writing across the product life cycle, focusing on Clinical Evaluation Plans/Reports and other CER-related documentation for Neuromodulation, CAHF and Vascular products. You will collaborate with R&D, Regulatory Affairs, Quality and Clinical teams to evaluate clinical evidence, manage CER projects, and ensure compliance with #J-18808-Ljbffr Abbott
$78k - $156k
...Maple GroveJob Type: Full timeCategory: Medical and Clinical AffairsIndustry: HealthcarePosted Date: 2... ...currently has an on-site opportunity for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides...SeniorRegulatoryWork experience placementWorldwide- Abbott Laboratories in Maple Grove, MN seeks a Senior Medical Writer, Clinical Evaluation, to provide technical and strategic writing across the product... ...lifecycle. You will author CERs/CEP and related regulatory documents for Neuromodulation, CAHF and Vascular products...SeniorRegulatory
- ...Laboratories in Maple Grove, MN seeks a Senior Manager, Study Data Architecture to lead... ...database configuration and governance for the clinical development portfolio on-site. You will... ..., and scalable data solutions for regulatory submissions and analytics. #J-18808-Ljbffr...SeniorRegulatory
- Abbott in Maple Grove, MN seeks a Senior Clinical Quality Associate to support Global Clinical Affairs in ensuring medical device and GCP compliance. This in-house role focuses... ..., audits, and cross-functional regulatory support. The candidate will work in a quality...SeniorRegulatory
- Boston Scientific is seeking a Senior Clinical Research Specialist to join the Urology Biostatistics and Real World Evidence team. The role... ...world data, builds cohorts, and ensures documentation meets regulatory and scientific standards. Hybrid role in Minnetonka, with...SeniorRegulatory
- Abbott Laboratories in Maple Grove, MN is seeking a Manager, Clinical Data Review to lead a data management team and ensure data integrity... ..., and dataset preparation for analysis, while upholding regulatory and quality standards. You'll drive RBQM activities, monitor performance...SeniorRegulatory
- Boston Scientific is seeking a Principal Clinical Quality Assurance Specialist to support the internal clinical QA program for the assigned... ...cross‑functional teams to ensure investigations comply with regulatory requirements, GCP and company policies, serving as QA...SeniorRegulatory
$150k - $175k
...in people's lives. Our medical devices, software and... ...development, and execution of clinical trials in... ...consistent with legal and regulatory standards and company... ...provide regular updates to senior leadership.Manage... ...including performance evaluations and development of employee...SeniorRegulatoryMinimum wageOngoing contractFull timeContract workTemporary workWork at officeLocal areaRemote workWorldwideNight shift3 days per week$82.6k
...Role We are looking for a Senior Clinical Research Specialist to join... ...ICD-10-PCS, CPT, etc.) and medical terminologies (SNOMED, LOINC... ...safety, quality assurance or regulatory affairs) or advanced degree... ...Boston Scientific continues to evaluate its policies and protocols regarding...SeniorRegulatoryHourly payWork experience placementWork at officeShift work3 days per week- ...of one or more multi-center clinical research studies. This position... ..., review of essential regulatory documents, and assessing site... ...• Strong knowledge base of medical terminology and anatomy/physiology... ...field; however, upon evaluation, equivalent related experience...SeniorRegulatoryLocal areaRemote work
$134k - $190k
...Clinical Affairs Team Member Imagine how your ideas and expertise can... ...curiosity and passion for evaluating data to increase access to pioneering... ...investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the...SeniorRegulatory- ...Medical Writer II We believe that great healthcare is an essential safeguard of... ...the development and execution of clinical, scientific, and regulatory documents and presentations for internal... ...plans and reports, clinical evaluation plans and reports, reports and study...RegulatoryFlexible hoursShift work
- ...Senior Clinical Scientist If you're the kind of Clinical Scientist who wants to own the story... ...role at the center of Clinical, R&D, Regulatory, Therapy Development, and Quality—where... ...grounded in anatomical, procedural, and medical parameters Identify gaps,...SeniorRegulatoryShift work
- ...manufacturing, such as manufacturing readiness, audits, and clinical builds to ensure a smooth transition and continuously accurate... .... Review and approve protocols, reports, and change orders. Evaluate regulatory impact of equipment changes prior to implementation. • NC...SeniorRegulatory
- ...full range of healthcare services that include Medical, Behavioral Health, Dental, and Substance Abuse. The Clinical Support Coordinator provides administrative and... ...Maintain confidentiality and compliance with all regulatory and organizational policies. Participate in...SeniorRegulatoryWork at office
$166.4k - $249.6k
...first — developing innovative medical technologies that improve... ....In this exciting role as a Senior Clinical Program Manager (CPM) , you... ...generate data that supports regulatory, clinical, and business objectives... ..., as appropriate, clinical evaluation documents to ensure...SeniorRegulatoryH1bLocal areaImmediate startFlexible hours- ...exciting opportunity for Senior System Design Quality... ...product development, regulatory and standards... ...management of next-generation medical devicesInternational standards... ...1 and IEC 62304. Uses clinical knowledge to influence... ...continues to evaluate its policies and protocols...SeniorRegulatoryHourly payRelocation packageShift work3 days per week
- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you... ...related discipline within the medical device industry, including R&D, Quality, Clinical, Medical Affairs or Biocompatibility... ...Scientific continues to evaluate its policies and protocols regarding...SeniorRegulatoryHourly payWork at officeLocal areaShift work3 days per week
$106k - $170k
ABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to... ...SUMMARYThis position is for overseeing clinical activities related to one or more clinical... ...reporting adverse events as required by regulatory bodies, reviewing adverse event trends,...SeniorRegulatoryWork experience placementInterim roleLocal areaFlexible hours$78k - $156k
...Maple GroveJob Type: Full timeCategory: Medical and Clinical AffairsIndustry: HealthcarePosted Date... ..., currently has an opportunity for a Senior Clinical Quality Associate. This... ...implementation reports · Ensure work complies with regulatory and compliance standards · Work cross-...SeniorRegulatoryWork experience placementLocal areaRemote workRelocation$85.1k - $161.7k
...are currently seeking an Epic Clinical Subject Matter Expert &... ...Consulting Services team. The Senior Associate will operate across... ...Epic Systems best practices, regulatory expectations, and long-term sustainability... ...; political affiliation; medical condition (including family...SeniorRegulatoryFull timeWork experience placementInternshipLocal areaImmediate start- ...Job Title: Medical Writer Client: Medical Device Manufacturing Company Duration: 12 Months Location: Maple Grove, MN, 55... ...Green Card Holder Only Key Words: CER (Clinical Evaluation Review/Report) Writing MDR (Medical Device Regulations...Contract workInterim roleFreelance
$137.7k
...About the Role Reporting to the Senior Director of Business... ...opportunities, conduct due diligence, evaluate potential deal structures... ...Marketing, Research, R&D, Clinical, Regulatory, and/or other functions as... ...Banking in the healthcare domain (medical device experience preferred)...SeniorRegulatoryHourly payRelocation packageShift work3 days per week$116.6k
...experience every day. As a Principal Clinical Quality Assurance Specialist,... ...comply with applicable regulatory requirements, Good Clinical... ...Scientific policies and procedures. Evaluate the accuracy, integrity and... ...lives through innovative medical technologies that improve the...RegulatoryHourly payLocal areaRelocationShift work3 days per week- ...employees experience every day.The Senior Product Manager, Hepatic... ...work closely with Sales, Medical Affairs, Clinical, Medical Education, Health Economics, Regulatory, Legal, and cross-functional... ...KPIs, and campaign metrics to evaluate business impact and refine commercial...SeniorRegulatoryHourly payWork at officeRelocationRelocation packageShift work3 days per week
$131k - $151k
...Anteris is seeking a Senior Usability/Human Factors... .... Prototyping & Evaluation Prototype novel solutions... ...with ISO and regulatory standards (e.g., FDA Human... ...engineering, marketing, clinical, and regulatory teams... ...usability engineering for medical devices. Experience...SeniorRegulatoryTemporary workH1bLocal areaVisa sponsorshipWork visaFlexible hours$110k
...an Interventional Solutions Senior Clinical Specialist, you will play a... ...policies, quality standards and regulatory requirements.... ...Minimum of 4 years' experience in medical device sales, healthcare, clinical... ...Boston Scientific continues to evaluate its policies and protocols...SeniorRegulatoryFull timeWork experience placementFlexible hours$137.7k
...experience every day. As a Senior Manager, you will lead the development... ...closely with Global Marketing, Medical Affairs, Clinical, R&D, Regulatory, Commercial and regional HEMA teams... ...analytical and strategic thinking to evaluate market dynamics, prioritize...SeniorRegulatoryHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior... ...Specialist, UltrasoundThe Senior Regulatory Affairs... ...offering strategic guidance on clinical studies and evaluations.Your role:Act as an ambassador... ...of Conformity, and Medical Device Licenses—for various...SeniorRegulatoryFull timeWork at officeImmediate startWork visaRelocation package3 days per week- ...progressing – whatever your ambitions. Senior Legal CounselAbout the Role:... ...while managing legal and regulatory risk. You will also help... ...regulations and guidance affecting the medical device industry.Participate... ...Scientific continues to evaluate its policies and protocols...SeniorRegulatoryHourly payFixed term contractWork at officeLocal areaShift work3 days per week
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