AEM Author TekWissen LLCAEM AuthorMalvern, PA$55Maintains broad awareness of changing technology, applications, trends, client needs, and legislative changes to proactively support creation and testing of marketing/communication content. Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.
Clinical Document Author - Remote YO AI LabsClinical Document Author - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Informed Consent Writer ICON PlcInformed Consent WriterBlue Bell, PAInformed Consent Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, custo...
Medical Writer II- #26-19501 US Tech Solutions, Inc.Medical Writer II- #26-19501Princeton, NJ$66–$77 / hourExcellent computer skills, with demonstrated expertise in the Microsoft suite (Word, Excel, PowerPoint, Teams, OneNote, Outlook) and Adobe Acrobat. US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.
Medical Writer / Clinical Document - Remote YO AI LabsMedical Writer / Clinical Document - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Manager, External Affairs Rocket Pharmaceuticals IncManager, External AffairsCranbury, NJ$120,000–$160,000 / yearThis role will support the execution of external communications initiatives by developing high-quality written materials, coordinating cross-functional projects, supporting scientific communications, and ensuring consistent messaging across external stakeholders. We encourage applicants with at least four years of relevant experience who demonstrate strong biotechnology or life sciences expertise, exceptional writing capabilities, and a record of successfully managing cross-functional communications initiatives to apply.
Manager, External Affairs Rocket PharmaceuticalsManager, External AffairsCranbury, New Jersey$120,000–$160,000 / yearFull timeThis role will support the execution of external communications initiatives by developing high-quality written materials, coordinating cross-functional projects, supporting scientific communications, and ensuring consistent messaging across external stakeholders. We encourage applicants with at least four years of relevant experience who demonstrate strong biotechnology or life sciences expertise, exceptional writing capabilities, and a record of successfully managing cross-functional communications initiatives to apply.
Senior Manager, Medical/Regulatory Writer Immunocore Holdings PlcSenior Manager, Medical/Regulatory WriterRadnor, PAVacancy NameSenior Manager, Medical/Regulatory Writer Vacancy NoVN831 Employment TypeFull Time Location of roleGaithersburg, MD, Radnor, PA, Remote, US DepartmentRegulatory Affairs Key ResponsibilitiesThe Senior Manager, Medical/Regulatory Writer will be accountable for leading and overseeing the medical and scientific regulatory writing for assigned programs to support submissions from first-in-human studies through product registration. Authoring or supervising the preparation of other regulatory documents required for Health Authority submissions, including but not limited to: Clinical Summaries (Clinical Overview, ISS/ISE, PK/PD summary, Advisory Committee Briefing document), Investigator Brochure(s), DSURs, other regulatory documents including briefing documents for health authorities, responses to Health Authority questions, etc.
NewSenior Medical Writer, Clinical and Regulatory Strategic Communications (CRSC) Merck & Co IncSenior Medical Writer, Clinical and Regulatory Strategic Communications (CRSC)North Wales, PA$117,000–$184,200 / yearDemonstrates independence in preparing clinical regulatory (e.g., protocols, clinical study reports, participant narratives, investigator's brochures) and/or public-facing (e.g., informed consent forms, clinical trial registration and results postings, plain language summaries) documents per company and evolving regulatory requirements. Applies emerging critical thinking, problem solving, and negotiation skills to implement solutions to challenges across the medical writing scope of work (e.g., documents, content, processes, timelines, tools) while navigating project team dynamics.
Medical Writer - Remote YO AI LabsMedical Writer - RemotePhiladelphia, PennsylvaniaRemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Senior Technical Writer - Madcap Flare & AI Expert Wolters KluwerSenior Technical Writer - Madcap Flare & AI ExpertPhiladelphia, PARemote$60,700–$106,000 / yearThis is an exciting opportunity for a technical writer who enjoys learning complex software, partnering with Product Managers and Subject Matter Experts, and turning complicated functionality into clear, intuitive documentation for end users. We've been recognized by employees as a European Diversity Leader in the Financial Times, as one of Forbes America's Best Employers for Diversity in 2022, 2021 and 2020 and as one of Forbes America's Best Employers for Women in 2021, 2020, 2019 and 2018.