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.
Contractor - AEM Author IMCS Group IncContractor - AEM AuthorMalvern, PAPerform all the authoring operations by leveraging the content management system (CMS) to edit, upload, delete, and manage content used online. Experience authoring webpages and administering digital assets using Adobe Experience.
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.
Medical Writer Position Integrated Resources, IncMedical Writer PositionCollegeville, PennsylvaniaContractorRESPONSIBILITIES: Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products. TECHNICAL KNOWLEDGE: Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy.
Medical Writer Integrated Resources, IncMedical WriterCollegeville, PennsylvaniaContractorRESPONSIBILITIES: Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products. TECHNICAL KNOWLEDGE: Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy.
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.
Medical Writer, Health Literacy Merck & Co IncMedical Writer, Health LiteracyNorth Wales, PA$96,200–$151,400 / yearDemonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical study reports, participant narratives, investigator's brochures) and/or public-facing (e.g., clinical trial registration and results postings, plain language summaries, informed consent forms) documents per company and evolving regulatory requirements. Preferred skills & experience for Health Literacy Writer: Experience in plain language authoring or communication, such as patient- or public-facing materials, informed consents, plain language summaries, or other health-literate clinical research materials.
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.
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.
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.