UNKNOWN

FEED

The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.

YEAR

SystImmune, Inc.

Medical Writer

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As part of Inizio Medical, our clients benefit from the synergies available within our global network of offices staffed by highly talented individuals who can deliver on a global scale or a local level and across a broad spectrum of therapy areas. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

HOUR

Nucleus Global Ltd

Lead Medical Writer

Working closely with internal teams and clients, youll translate complex clinical data into clear, compelling narratives that support payer engagement and brand success. As a Medical Writer, Market Access , you will play a critical role in developing strategic, scientifically accurate content that drives brand differentiation and maximizes access goals.

GLE Creative Talent

Market Access Medical Writer

RESPONSIBILITIES: Working with the Executive Director, Regulatory and Medical Writing, lead the development, authoring, and delivery of complex regulatory documents such as clinical study reports and marketing application summary documents (Module 2), and lead and/or contribute to Investigator's Brochures, clinical study protocols, and briefing documents. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.

Ionis Pharmaceuticals Inc

Associate Director, Regulatory and Medical Writer

He or she is also responsible for the messaging strategy across a program of work, for the provision of strategic input into the development of clinical development plans and submission plans, and for analyzing proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Plasma

Principal Medical Writer

The purpose of this job is to support clinical evaluation reports (CERs) per Medical Device Regulation (MDR), to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, recertification and proposed indication/labeling changes, as well as CER updates to maintain EU product conformance. Competency Requirements: (Competency is based on: education, training, skills and experience.)In order to adequately perform the responsibilities of this position the individual must: " Previous experience in the application of therapeutic and device knowledge to support the development of clinical evaluation reports.

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eTeam Inc.

Medical Writer 2

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Position Summary: The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Key Responsibilities: Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.

Systimmune Inc

You actively use tools such as ChatGPT, Claude, or AI-assisted research and writing platforms to improve how you work and can clearly articulate how they enhance output quality and efficiency — while maintaining scientific integrity and compliance. Provide mentorship, training, and editorial guidance to junior Medical Writers and Editors, supporting their development and helping the team consistently deliver high-quality work.

MJH Life Sciences

Reporting directly to the Chief Medical Officer, this individual will lead the writing of clinical study reports, regulatory submissions, and scientific communications in support of the company's Phase II and Phase III clinical trial programs. The Role: The Medical Writer will serve as an important contributor to Sagimet Biosciences' Clinical and Regulatory Affairs teams, responsible for the creation, coordination, and delivery of high-quality clinical and regulatory documents.

Sagimet Biosciences Inc

Senior Medical Writer

Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Precision AQ

Senior Medical Writer, Medical Communications

PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Medpace Holdings Inc

Medical Writer PhD Cardiovascular/Metabolic Cincinnati

PhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Medical Writer PhD Hematology/Oncology Cincinnati

Knowledge, Skills and Abilities: Have a demonstrated ability to produce clear, concise, and effective written and verbal communications describing scientific and clinical data in English. An independently motivated working style with good problem-solving skills that allow analysis, synthesis, and compilation of data from a broad range of disciplines.

Mirum Pharmaceuticals Inc

Researches, authors, and/or edits complex clinical, scientific, and program-level regulatory documents, which may include Investigator's Brochures (IBs), Investigational New Drug (IND) application documents, and Marketing Authorization Application (MAA) documents. Serves as a primary author, providing strategic input and authoring regulatory documents supporting Phase 1 3 clinical drug development, including clinical study protocols, protocol amendments, and Clinical Study Reports (CSRs).

Katalyst Healthcares & Life Sciences

AdMed is an award winning, integrated agency that designs and delivers modern training tools for pharmaceutical, biotech, diagnostic and medical products, with one goal: to ensure that healthcare professionals, sales teams, employees and consumers understand what they need to know regarding the science behind their products. The role involves all stages in the development of AdMed’s products – from brainstorming with clients, to researching and writing original content, to acting as a virtual teacher in video training programs.

AdMed Inc.

Medical Writer - Hybrid Role

Regardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.

FULL_TIME

OTHER

Force Medical Communications

Medical Writer, Medical Communications

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Responsibilities / Position overview: We are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical Strategy and Communications team, which serves our clients by mobilizing our scientific knowledge to interpret the data and create compelling narratives to guide their medical strategy and through regulatory challenges. The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts), slide decks, scientific platforms, symposia, advisory boards, and training materials.

Lumanity

[AW]-iCims

You will serve as a key contributor to manuscript development, congress activities, publication project management, and scientific communications initiatives, partnering closely with Medical Affairs North America, Global Scientific Communications, Value & Evidence and other cross-functional partners, as well as external authors. As a Senior Medical Communications Writer on the Medical Affairs, North America team, you will be responsible for researching, writing, and editing scientific publications and communications materials that advance the understanding of rare MC4R pathway diseases and support Rhythm’s medical communications objectives.

Medical Writer Jobs in the United States

Medical Writer SystImmune, Inc.

Lead Medical Writer Nucleus Global Ltd

Market Access Medical Writer GLE Creative Talent

Associate Director, Regulatory and Medical Writer Ionis Pharmaceuticals Inc

Principal Medical Writer CSL Plasma

Medical Writer 2 eTeam Inc.

Medical Writer Systimmune Inc

Principal Medical Writer MJH Life Sciences

Senior Medical Writer Sagimet Biosciences Inc

Senior Medical Writer Nucleus Global Ltd

Senior Medical Writer, Medical Communications Precision AQ

Medical Writer PhD Cardiovascular/Metabolic Cincinnati Medpace Holdings Inc

Medical Writer PhD Hematology/Oncology Cincinnati Medpace Holdings Inc

Principal Medical Writer Mirum Pharmaceuticals Inc

Senior Medical Writer Katalyst Healthcares & Life Sciences

Medical Writer - Hybrid Role AdMed Inc.

Medical Writer Nucleus Global Ltd

Medical Writer, Medical Communications Force Medical Communications

Senior Medical Writer Lumanity

Senior Medical Communications Writer - Medical Affairs, North America Rhythm Pharmaceuticals

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