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    London, Greater London, United Kingdom Langland Full time

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    London, Greater London, United Kingdom Langland Full time

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  • Medical Writer

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    London, Greater London, United Kingdom Langland Full time

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  • Medical Writer

    6 days ago

    London, Greater London, United Kingdom Langland Full time

    {"title": "Medical Writer", "content": "Job SummaryWe are seeking a skilled Medical Writer to join our team at Langland. As a Medical Writer, you will be responsible for creating high-quality, scientifically sound content for our clients. This is an exciting opportunity to work with a talented team and contribute to the development of innovative medical...

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  • Medical Writer

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    London, Greater London, United Kingdom Publicis Denmark AS Full time

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    London, Greater London, United Kingdom Lumanity Full time

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  • Medical Writer

    7 days ago

    London, Greater London, United Kingdom Lumanity Full time

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  • Medical Writer

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    London, Greater London, United Kingdom Publicis Denmark AS Full time

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  • Medical Writer

    7 days ago

    London, Greater London, United Kingdom Publicis Denmark AS Full time

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  • Medical Writer

    1 week ago

    London, Greater London, United Kingdom Publicis Groupe UK Full time

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  • Medical Writer

    1 week ago

    London, Greater London, United Kingdom Publicis Groupe UK Full time

    Medical Writer Job DescriptionLangland, a Publicis Health company, is a leading health communications agency that thinks further across Clinical Trial Experience, Medical Strategy & Education, Public Relations & Policy, and Advertising, to create unique value with visionary clients.We are seeking a talented Medical Writer to join our Medical Strategy &...

Medical Writer

4 months ago

London, Greater London, United Kingdom Remote Worker Ltd Full time

We have a fantastic opportunity for a Medical Writer to join our Medical Device Client working across their extensive portfolio of products. The business is passionately committed to partnering with medical professionals to help elevate the delivery of patient care and improve clinical outcomes, and this role will suit someone who is experienced in CER's, CEP's and PMCF's. Remote working is also on offer

Responsibilities Conduct scientific literature reviews and compile reports, such as annual literature updates and periodic safety updates, to provide to global regulatory agencies Generate protocols and reports using a well-defined scientific/research methodology Write and contribute to Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Follow-Up Plans and Reports, and Summaries of Safety and Clinical Performance supporting multiple products Write Post Market Surveillance Plans and reports Provide clinical input for updating the Instructions For Use (IFU) and Risk Assessments Collaborate with team on responses to questions / requests for more information from reviewers and auditors regarding these documents Conduct ad hoc literature reviews and data synthesis as required to address the questions referenced above Create and maintain standard operating procedures and work instructions for preparation and maintenance of compliant medical writing deliverablesSkills and experience Scientific background (BS or above in Biology, Chemistry, Biomedical Engineering, or related field) Experience conducting systematic literature reviews for medical devices required (experience with medical databases such as Pubmed preferred) Experience writing or contributing to Clinical Evaluation Reports compliant with MEDDEV 2.7/1 rev 4 required Experience with MDD essential. MDR experience preferred Knowledge of ISO (phone number removed) and 10993 series of standards preferred but not essential Must have excellent written and verbal communication skills Must have an ability to work to deadlines, be self-motivated and well organised Experience writing or contributing to Clinical Evaluation Reports compliant with EU MDR 2017/745 desired Ability to understand and interpret results of clinical studies, with a strong understanding of statistics Expertise in conducting focused literature searches on PubMed, MedLine or other similar literature databases Effective written and oral communication skills Ability to formulate reports and present findings Ability to prioritize and manage multiple projects Strong familiarity with Microsoft Office Data-mining and analysis skills.For immediate consideration please forward your most up to date CV Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status. Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants. Check us out on our and for more roles. We respect your personal data and would never offer it to third parties For more information on how we handle your data, feel free to check out the or contact (url removed) Austin Fraser International Ltd is registered in England: (phone number removed) Austin Fraser International Ltd, 33 Soho Square, London, W1D 3QU Seniority level
  • Seniority level Entry level
Employment type
  • Employment type Full-time
Job function
  • Job function Marketing, Public Relations, and Writing/Editing
  • Industries Staffing and Recruiting

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