The Medical Writer is responsible for developing high-quality clinical documentation, including site manuals and charters, while ensuring compliance with regulatory standards. They will review study protocols, eCRFs, and SOPs to maintain accuracy and consistency across clinical studies.
Remote Medical Writer Jobs (102)
Search = Medical Writer
The role involves writing and updating Clinical Evaluation Reports (CERs), PMCF reports, and SSCPs to comply with international regulations. It also requires analyzing clinical data and collaborating with cross-functional partners to respond to regulatory agency requests.
The Medical Writer creates high-quality scientific and clinical content for healthcare providers across various digital and in-person formats. They collaborate with medical experts and internal teams to develop instructionally sound medical education programs.
Develop, write, and edit high-quality clinical and regulatory documentation to support the development and registration of medical devices. Collaborate with cross-functional teams to interpret clinical data and ensure compliance with global regulatory standards.
Lead the planning, writing, and editing of high-quality regulatory documents including CSRs, IBs, and eCTD summaries for clinical drug development. Collaborate with cross-functional teams to analyze scientific data and respond to health authority requests.
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The primary role involves developing accurate, high-quality, and compliant medical and scientific content based on clinical data, publications, and medical insights. This includes creating various materials like slide decks, manuscripts, and medical information pieces while ensuring scientific accuracy and adherence to standards.
The primary role involves developing accurate, high-quality, and compliant medical and scientific content based on clinical data, publications, and medical insights. This includes creating various materials like slide decks, manuscripts, and medical information pieces while ensuring scientific accuracy and adherence to standards.
The Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
Lead the development of high-quality regulatory and clinical documents, including clinical study reports and protocols. Oversee medical writing workstreams and mentor junior writers to ensure adherence to industry standards and timelines.
Senior/Principal Medical Writer - Canada
Trilogy Writing and Consulting
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Full Time
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3 Days Ago
Trilogy Writing and Consulting
Lead the preparation of clinical regulatory documents such as protocols, study reports, and summaries in collaboration with client teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.
Principal Medical Writer, Brand & Promotion
AQ International
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Full Time
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3 Days Ago
AQ International
Lead the development of high-quality, ABPI-compliant promotional content and brand narratives across multiple digital and print channels. Act as the scientific expert in client-facing discussions and navigate the medical-legal-regulatory (MLR) review process.
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos Health
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Full Time
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4 Days Ago
Syneos Health
Develop global regulatory submission documents including Clinical Study Reports and Clinical Overviews in accordance with ICH guidelines. Manage medical writing projects by developing timelines and coordinating with cross-functional teams to meet corporate objectives.
Develop and deliver high-quality scientific content, including abstracts, posters, and manuscripts, for a global publications account. Build long-term client relationships and identify opportunities for organic growth within the oncology and hematology therapy areas.
Senior Medical Writer (Publications) North America
Thermo Fisher Scientific
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Full Time
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5 Days Ago
Thermo Fisher Scientific
The role involves senior-level medical writing focused on publications within the North American region. The candidate will be responsible for creating and managing scientific documents and publications.
Senior Medical Writer - US/Europe - Remote
Worldwide Clinical Trials
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Full Time
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5 Days Ago
Worldwide Clinical Trials
Lead the medical writing team in preparing Phase I-IV study documents, including protocols, clinical trial reports, and investigator brochures. Collaborate with subject matter experts to develop Pre-IND documents and briefing books for global regulatory authorities.
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the company pipeline. This role also involves mentoring other medical writers and leading process optimization for departmental tools and templates.
Lead the delivery of medical communications projects, ensuring high-quality, on-time, and on-budget deliverables for clients. Manage and mentor junior medical writers while shaping client strategy and maintaining deep therapeutic area expertise.
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Lead the preparation and review of clinical study documents, including protocols, CSRs, and regulatory submissions. Collaborate with cross-functional teams to analyze clinical trial data and mentor junior medical writers to ensure high-quality scientific output.
Review and develop AI-drafted manuscripts for pharmaceutical clients to ensure high-quality clinical trial publications. Liaise with authors to move manuscripts toward submission while adhering to strict confidentiality and data privacy parameters.
Develop high-quality scientific content and lead publications and medical affairs strategies for global oncology clients. Mentor junior medical writers and maintain strong relationships with clients and authors.
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the oncology pipeline. This role also involves mentoring other medical writers and leading the optimization of departmental processes and templates.
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the oncology pipeline. This role involves leading document strategy, managing timelines for complex submissions, and mentoring junior medical writers.
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. This involves analyzing and presenting scientific and statistical information according to ICH and company standards.
Develop high-quality scientific content and partner with global clients on medical affairs and commercial strategies for neurologic diseases. The role also involves coaching junior writers and co-leading scientific meetings and client calls.
The Senior Medical Writer is responsible for authoring and editing complex clinical development documents, including protocols and study reports, while ensuring scientific rigor. They will manage project timelines, coordinate directly with clients, and mentor junior medical writers.
The Medical Writer is responsible for authoring and editing critical clinical development documents, including protocols, investigator's brochures, and clinical study reports. They will manage project timelines, coordinate directly with clients, and mentor other medical writers within the team.
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Medical Writer - Senior Regulatory Writing Specialist (Clinical)
Med Communications International
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Full Time
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1 Week Ago
Med Communications International
Responsible for creating regulatory materials for investigational and marketed products in alignment with compliance practices. The role involves managing regulatory writing projects and leading cross-functional review meetings to ensure document accuracy.
Senior Medical Writer - Regulatory Documents - CSR /Protocol - Late Phase
Syneos Health
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Full Time
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1 Week Ago
Syneos Health
Leads the creation and accurate completion of regulatory medical writing deliverables, including protocols and clinical study reports. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and are delivered on time.
Medical Writer I (Junior Project Specialist - 1 year Contract)
Syneos Health
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Full Time
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2 Weeks Ago
Syneos Health
The role involves managing compliant document filing and eTMF activities within the Veeva RIM system. It also requires maintaining project timelines and collaborating with stakeholders to ensure regulatory standards are met.
The Associate Medical Writer is responsible for creating and formatting various medical documents while adhering to regulatory guidelines and QC processes. They will manage projects from start to finish, handle client feedback, and mitigate project risks.
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