To support the development of clinical, scientific, and regulatory documents, the remote UK Medical Writer will create and edit reports in compliance with regulatory standards while collaborating with cross-functional teams and conducting literature reviews. Key responsibilities Assess clinical data to verify scientific validity, clinical performance, and safety of medical devices Prepare and review regulatory Clinical Regulatory Reports, including Clinical Evaluations and Post Market Surveillance documents Conduct literature searches and collaborate with teams to analyze clinical and safety data Required qualifications 0-2 years of experience in medical writing or related fields Bachelor's, Master's, or Ph.D. degree in a relevant area Strong medical and technical writing skills Familiarity with research software and databases, such as Endnote and PubMed Ability to work independently and manage multiple projects effectively
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