Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical Evaluation Medical Writer- Remote

Careers Integrated Resources Inc

New York, NY
  • Remote job

Clin Evaluation Med Writer Job Location: Virtual, MN Duration: 12 Months Shift Schedule: 1st Shift Summary: The Senior Clinical Evaluation Medical Writer is responsible for authoring, reviewing, and managing clinical evaluation documents and reports in compliance with regulatory requirements and industry standards. This role involves synthesizing clinical data, scientific literature, and regulatory guidelines to create clear, concise, and evidence-based documentation that supports the safety and performance of medical devices. The writer collaborates closely with cross-functional teams to ensure the timely delivery of high-quality clinical evaluation reports (CERs) and related documents. Strong analytical skills, attention to detail, and the ability to communicate complex medical and scientific information effectively are essential for success in this role. Responsibilities: Review and summarize scientific literature. Appraise, analyze, summarize, and discuss clinical evidence from all available sources. Conduct comprehensive literature searches and perform critical evaluation of clinical evidence. Maintain a database of peer-reviewed literature. Develop state of the art (SOTA) on product family for its intended purpose. Create and maintain plans and reports for regulatory authorities, including Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), Post-Market Clinical Follow-up Plans (ProductF-P), Post-Market Clinical Follow-up Reports (ProductF-R), Summary of Safety and Clinical Performance (SSCP), Periodic Safety Update Reports (PSUR). Report instances of complaints/adverse events from literature. Create responses for audit/submission queries. Required Skills: Knowledge of regulatory agencies' guidelines on clinical evaluation requirements. Experience writing clinical evaluation documents. Medical Device experience. Strong project management skills. Strong communication skills. Ability to deliver and manage projects assigned and work with other stakeholders to achieve desired results. Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A)) and a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years relevant experience. Careers Integrated Resources Inc

Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Clinical Evaluation Medical Writer- Remote in New York, NY vacancy
  • $78k - $156k

     ...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 1...  ...currently has an on-site opportunity for a Senior Medical Writer, Clinical Evaluation. The Sr. Medical Writer on our Regulatory Clinical... 
    Suggested
    Work experience placement
    Worldwide
    Shift work

    Abbott

    Maple Grove, MN
    2 days ago
  •  ...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...  ...toxic light chains. NXC-201 is being evaluated in the U.S. multi-center study for relapsed... 
    Remote work
    Odd job

    Immix Biopharma (Nasdaq: IMMX)

    West Virginia
    10 days ago
  • MMS Holdings Inc is seeking an experienced Medical Writer based in Denver, Colorado. The role involves writing and editing clinical documents, evaluating medical literature, and mentoring team members. A strong background in regulatory writing and at least 3 years of experience... 
    Remote job

    MMS Holdings Inc

    Denver, CO
    1 day ago
  • $50 - $80 per hour

     ...Role Overview Apply regulatory medical writing expertise to author and evaluate clinical documentation used to train and assess AI-assisted writing tools. In...  ...Terms Engagement type: Contractor. Location: Remote. Project focus: Contributing to a client project... 
    Remote work
    Hourly pay
    For contractors

    SaidGig

    United States
    more than 2 months ago
  • MMS Holdings Inc in Austin, Texas seeks a skilled Medical Writer to evaluate medical literature and write essential clinical documents. Candidates should have 3-5 years of regulatory writing experience within the pharmaceutical industry. The Medical Writer is responsible... 
    Remote job

    MMS Holdings Inc

    Austin, TX
    1 day ago
  • AuraOne is seeking a Medical Writer (Pharmaceutical) for a remote contractor role to evaluate AI outputs that touch pharma. You will review clinical reasoning, dosing logic, and guideline adherence, flag patient-safety issues, and document corrected reasoning for the modeling... 
    Remote job
    For contractors

    AuraOne

    New York, NY
    2 days ago
  •  ...Abbott seeks a Senior Medical Writer / Senior Project Manager, Clinical Evaluation to support EU regulatory submissions for vascular medical devices. The role combines clinical evidence evaluation, regulatory documentation authoring, and cross-functional project coordination... 

    Abbott

    Saint Paul, MN
    16 days ago
  • **Senior Medical Writer / Senior Project Manager, Clinical Evaluation****Working at Abbott**At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:* Career development... 
    Worldwide
    Shift work

    Thornton Tomasetti

    Santa Clara, CA
    3 days ago
  • Medical Writer (Consultant) - Clinical Development / Early Feasibility Study Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates residing in Europe are also encouraged to...  ...Study Context The program will: Evaluate proof of concept and efficacy of the... 
    Remote work
    Contract work
    Immediate start

    Confidential

    Seattle, WA
    4 days ago
  • Abbott is seeking a Senior Medical Writer / Senior Project Manager, Clinical Evaluation, to join the Vascular Division on-site in Santa Clara, CA or Maple Grove, MN. The role combines clinical evaluation expertise with project leadership to support regulatory submissions... 

    Thornton Tomasetti

    Santa Clara, CA
    3 days ago
  • To support clinical evaluation efforts, the contract Medical Writer with Clinical Focus will work remotely, authoring Clinical Evaluation Reports (CERs) and conducting literature reviews to ensure compliance with Medical Device Regulation (MDR) requirements. Key responsibilities... 
    Remote work
    Contract work

    Virtual Vocations Inc

    New York, NY
    5 days ago
  • FitOn is looking for a licensed Nurse Practitioner to serve as a Clinical Chart Reviewer. This remote role requires conducting patient evaluations and reviewing clinical documentation. The ideal candidate will have a strong focus on ensuring effective and evidence-based... 
    Remote job

    kozmetickesluzby.vecnakraska.sk - Jobboard

    Tampa, FL
    4 days ago
  • $45 - $65 per hour

    Gridnaut Recruiting is hiring a remote Certified Medical Coder (ICD-10) — Multilingual Clinical Documentation & AI Evaluation contractor (pay $45-$65/hr). Contribute to frontier AI research and evaluation work. Ideal candidates: Remote contractor engagement supporting a... 
    Remote work
    Hourly pay
    Temporary work
    For contractors

    Gridnaut Recruiting

    Remote
    a month ago
  • Regeneron Pharmaceuticals, Inc. seeks a Medical Writer to join Global Clinical Development in a remote work model in the United States. You will develop clinical study documents and support timely, compliant delivery across therapeutic areas, collaborating with cross-functional... 
    Remote job

    Regeneron Pharmaceuticals

    New York, NY
    4 days ago
  • MMS, a data-focused CRO, is seeking an experienced Medical Writer to critically assess literature, craft clinical development documents, and manage writing projects for regulatory submissions. The role requires leadership of project teams, strong communication with clients... 
    Remote job

    MMS

    New York, NY
    5 days ago
  • BioMarin Pharmaceutical Inc. is seeking a Principal Clinical Medical Writer to lead the medical writing function within Development Sciences. The role emphasizes reducing CRO costs, increasing writing productivity, and ensuring consistent documentation quality across programs... 
    Remote job

    BioMarin Pharmaceutical

    New York, NY
    2 days ago
  • Interpreting complex clinical study protocols, the full-time Clinical Trials Medical Writer will prepare and coordinate laboratory specifications and medical documents...  ...while collaborating with internal departments in a remote role based on the East Coast. Key... 
    Remote work
    Full time
    Work at office

    Virtual Vocations Inc

    New York, NY
    1 day ago
  • SaidGig seeks medical experts to remotely craft advanced AI evaluation content. You will create challenging medical Q&A pairs, verify answers against primary literature...  ...clear reasoning. The role emphasizes synthesis and clinical reasoning, with task-based work and prompt... 
    Remote job

    SaidGig

    New York, NY
    3 days ago
  •  ...Medical writer supporting clinical development across therapeutic areas. Responsible for creating and managing clinical study documents, protocols,...  ...submissions while collaborating with cross-functional teams in a remote U.S. position. Responsibilities Develop clinical... 
    Remote work

    Regeneron

    Remote
    6 days ago
  • MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and... 
    Remote job

    MMS Holdings

    New York, NY
    1 day ago
  • Rochester Regional Health is seeking a Medical Writer to interpret complex clinical study protocols and draft laboratory specifications and study documents for ACM Global Laboratories. You will collaborate with internal teams to draft, review, edit, and finalize technical... 
    Remote job

    ACM Medical Labs, Inc

    New York, NY
    3 days ago
  • MMS Holdings Inc, based in Michigan, is seeking an experienced Medical Writer to take on critical analysis and writing responsibilities for clinical development documents. The ideal candidate will have 3-5 years of experience in regulatory writing and anticipate working... 
    Remote job

    MMS Holdings Inc

    Lansing, MI
    5 days ago
  • Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. The Principal Medical Writer will lead clinical documentation efforts and manage complex regulatory submissions. They will collaborate with cross... 
    Remote job
    Worldwide

    [Unlock with Premium]

    New York, NY
    4 days ago
  • A leading medical device company is seeking a Medical Writer to develop clinical documents for an innovative project. This role focuses on drafting a Clinical Development...  .... and Europe are encouraged to apply. This is a remote role with an initial contract of 6-12 months. #J... 
    Remote job
    Contract work

    Confidential

    New York, NY
    1 day ago
  • ## Principal Medical Writer - Clinical FocusApply: Fully Remote: Massachusetts: Canada: United States: Full time: Posted Today: R-202609895**Job Description:****Position specific overview**Medical Writers prepare high quality documentation for regulatory submissions in... 
    Remote work
    Full time
    Local area
    Worldwide
    Flexible hours

    Veristat

    Eastern, KY
    5 days ago
  • $109.9k - $179.3k

     ...medicines for people with serious diseases. We are seeking a Medical Writer - Global Clinical Development, to join our Medical Writing team, supporting our clinical development organization in a remote work model. In this role, you will develop clinical study... 
    Remote work
    Worldwide

    Regeneron

    Remote
    7 days ago
  • $45 - $65 per hour

     ...Mercor is hiring certified medical coders on behalf of a healthcare...  ...AI partner building advanced clinical documentation tools. In this...  ...to review, annotate, and evaluate clinical documentation and AI...  ...reviews Work Arrangement Remote, part-time — minimum 10 hours... 
    Remote work
    Hourly pay
    Temporary work
    Part time
    Work experience placement
    10 hours per week
    Flexible hours

    Mercor

    San Francisco, CA
    7 days ago
  • $77k - $92k

     ...Job Title: Medical Writer Department: Study Set Up Location: Remote East Coast | Must Sit in East Coast Hours Per Week: 40 hours Schedule: Days,...  ...Medical Writer is responsible for interpreting complex clinical study protocols and other medical/scientific... 
    Remote work
    Hourly pay
    Full time
    Work at office
    Local area
    Monday to Friday
    Flexible hours

    Rochester Regional Health

    Remote
    7 days ago
  • Syneos Health, Inc. is seeking a Senior Medical Writer (FSP) with proven experience in clinical document writing, including protocols, CSRs, and IBs. The role...  ...quality documents on schedule. The position supports remote work with flexibility across EST/CST time zones and... 
    Remote job

    Syneos Health, Inc.

    New York, NY
    2 days ago
  • Regeneron Pharmaceuticals Inc. is seeking a Medical Writer to develop clinical documents including reports, protocols, and narratives. You will lead...  ...coordinate with Medical Writing leads, and drive timelines in a remote US setting. Ideal candidates hold a bachelor’s degree (... 
    Remote job

    Regeneron Pharmaceuticals

    New York, NY
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical Evaluation Medical Writer- Remote. Be the first to apply!