CLINICAL WRITER jobs in EUROPE ENGLAND, United Kingdom

? We have an exciting opportunity for a diligent, enthusiastic, and detail-orientated Clinical Writer to join our Editorial team. In... and fixed-term maternity cover vacancies. To learn more about the role of a clinical writer see: Requirements: A pharmacy...

and scientific innovation for generations to come. The role: We are seeking an experienced Clinical Trial Protocol Writer... of commitment, responsibility, and the resilience needed to achieve excellence. Job Summary: We are establishing a clinical...

and scientific innovation for generations to come. The role: We are seeking a Clinical Trial Grant Writer to support our dynamic... of commitment, responsibility, and the resilience needed to achieve excellence. Job Summary: We are establishing a clinical...

Reference Number: JO-2405-535110 Principal Medical Writer Rate: Negotiable Job Type: Permanent Location: High... Wycombe Principal Medical Writer High Wycombe Hybrid working model – Applicants must be willing to travel into the...

Reference Number: JO-2405-534093 Principal Medical Writer Rate: Negotiable Job Type: Permanent Location: Brighton... Senior/Principal Medical Writer Boutique medical communications business Location: Brighton – fully remote working...

that thinks further across Clinical Trial Experience, Medical Strategy & Education, Public Relations & Policy, and Advertising... crafts: science, strategy and creativity. Job Description As a Senior Medical Writer II working within Langland's Medical...

that thinks further across Clinical Trial Experience, Medical Strategy & Education, Public Relations & Policy, and Advertising... crafts: science, strategy and creativity. Job Description As a Senior Medical Writer II working within Langland's Medical...

Job Summary We are currently seeking a full-time, office-based Proposal Writer to join our Proposal and Feasibility... Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical...

Proclinical is seeking a Medical Regulatory Associate Director - Medical Writer who is passionate..., maintaining clinical information, and supporting various medical functions. Fluency in French is a key requirement for this role...

a Medical Writer, native Swedish speaker to join our team for 3 months. Additionally, we welcome applicants based in London... or those interested in remote work from Sweden as we are looking for a medical writer who has expertise in healthcare and pharmaceutical...

Writer, you will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs... Writer, you’ll have the opportunity to work on a diverse range of projects, from writing and editing clinical regulatory...

remote work from Turkey as we are looking for a medical writer who has expertise in healthcare and pharmaceutical industries... by translating complex scientific and clinical information into clear and concise documents. Their primary responsibility...

This is an opportunity for a Principal Medical Writer to join a flourishing medical education agency and be based in... their Buckinghamshire office. The Principal Medical Writer will be responsible for editorial development of educational materials...

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select... and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical...

Technical Competencies Required Experience as a clinical/regulatory/safety Medical Writer, e.g. preparation of a wide...Title: Medical Writer H/F Company: Ipsen Biopharm Ltd Job Description: Summary / purpose of the position...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency... or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze...

Responsibilities Writes clear and concise clinical submission documents, including clinical study reports, protocols..., clinical overviews, investigator brochures, and summary documents; experience with late-stage health authority responses...