Lead the development of high-quality regulatory and clinical documents to support submissions to regulatory authorities. Coordinate writing assignments, formulate strategies, and ensure compliance with industry standards and sponsor requirements.
Remote Medical Writer Jobs (139)
Search = Medical Writer
The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
Lead the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinate with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.
Develop clear and accurate scientific content across various medical communication deliverables while ensuring strategic alignment and scientific integrity. Lead assigned projects, manage client expectations, and mentor junior medical writers.
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They are responsible for analyzing and presenting scientific and statistical information in accordance with ICH and regulatory guidelines.
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Senior Regulatory Medical Writer, Client-embedded, FSP
Thermo Fisher Scientific
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Full Time
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6 Weeks Ago
Thermo Fisher Scientific
The Senior Medical Writer authors routine and complex clinical regulatory documents, including study reports, protocols, and INDs. They collaborate with cross-functional teams to ensure document accuracy and mentor junior medical writers to maintain high-quality deliverables.
Lead the development of clinical study documents and regulatory submissions while collaborating with cross-functional teams to analyze trial data. Provide strategic input for clinical development programs and mentor junior medical writers to ensure high-quality scientific output.
The Principal Medical Writer will lead the development of high-quality scientific content across various therapeutic areas and ensure compliance with industry standards. Responsibilities include conducting literature reviews, managing writers, and preparing materials for promotional review processes.
Associate Director, Medical Writer
MannKind Corporation
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Full Time
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7 Weeks Ago
MannKind Corporation
Lead the preparation and production of high-quality, ICH-compliant regulatory and scientific documents including protocols, CSRs, and submission documents. Coordinate cross-functional teams to ensure alignment with corporate milestones and maintain global regulatory compliance.
The Senior Medical Writer leads the development and scientific integrity of medical content for pharmaceutical and medical device clients. This includes conducting literature research, creating scientific copy, and collaborating with cross-functional teams to ensure regulatory compliance.
The role involves researching, writing, and editing scientific manuscripts, abstracts, posters, and slide presentations for the life sciences industry. The writer will collaborate with the Medical Communications team to deliver high-quality scientific content within designated deadlines.
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.
The Senior Medical Writer is responsible for authoring and editing complex clinical development documents, including protocols and regulatory summaries. They must manage project timelines, coordinate directly with clients, and mentor junior medical writers.
Create and develop medical-scientific content and training concepts for the Medudy platform, focusing on digital learning and video formats. Collaborate with experts to implement AI-supported workflows and ensure high scientific standards through rigorous fact-checking.
Senior/Principal Medical Writer - Canada
Trilogy Writing and Consulting
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Full Time
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9 Weeks 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.
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.
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.
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 involves leading document strategy, managing timelines for complex submissions, and mentoring junior medical writers.
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.
Lead and manage medical writing activities for clinical studies, including the development of manuscripts, abstracts, and posters. Coordinate with cross-functional teams to ensure scientific accuracy and adherence to regulatory standards and branding.
Senior Medical Writer, Promotional Review
Thermo Fisher Scientific
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Full Time
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11 Weeks Ago
Thermo Fisher Scientific
Perform high-quality medical review of promotional and non-promotional materials to ensure clinical accuracy and compliance with FDA-OPDP requirements. Author medical information documents such as Standard Response Letters and FAQs while providing mentorship to junior writers.
The Senior Medical Writer designs and develops scientifically accurate materials such as slide decks, manuscripts, and website copy for various audiences. They manage client relationships, lead communications, and provide basic reviews and feedback to junior team members.
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Senior/Principal Medical Writer
Trilogy Writing and Consulting
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Full Time
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12 Weeks Ago
Trilogy Writing and Consulting
Lead the preparation of various clinical regulatory documents and scientific publications in collaboration with client authoring teams. Manage project timelines, budgets, and review cycles while overseeing other writers and QC specialists.
The Senior Medical Writer is responsible for preparing critical regulatory documents including IND applications, clinical study protocols, and investigator's brochures for oncology trials. The role involves collaborating directly with clients, medical monitors, and senior leadership to manage document timelines and review cycles.
Lead the development of high-quality regulatory and clinical documents to support submissions to global regulatory authorities. Manage medical writing projects, including timeline development and cross-functional coordination to ensure compliance with industry standards.
Lead the development of high-quality regulatory and clinical documents to support client submissions to regulatory authorities. Coordinate writing assignments, formulate strategies, and provide functional guidance on international regulatory requirements.
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