MLR Technical Reviewer Location: Spain / Europe Level: Academia / Mid-level The MLR Technical Reviewer will be responsible for the scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets for our major pharmaceutical firm globally. The MLR Technical Reviewer will work in an international and cross-functional environment, following general and local guidelines and working closely with internal and external stakeholders to ensure the highest quality for the companies assets and gathering data on asset quality and agency performance. Responsibilities Perform data/referencing quality checks of scientific/medical assets; ensuring all content is scientifically accurate and appropriately supported by the Reference Documents Review content and identify any non-compliances with the local regulatory guides Perform some actions in the Review and Approval platform (Veeva Vault)
such as reference tagging or claims object creation Check anchors/links to references required to support the scientific/medical assets Identify assets that may require pre-alignment with internal stakeholders Flag claims that may be difficult to substantiate or do not follow regulatory/internal guidelines Track asset quality data for internal and external reporting Requirements Experienced Medical Writer from academia or a commercial role with experience in Medical Content Reviewing or a strong scientific background and degree (Pharm D, MD, Ph D or Master's) Excellent medical writing skills Strong attention to detail and accuracy, ability to manage and prioritise multiple, detailed activities, results-oriented with fast and focused execution Good communication, coordination and time management skills Fluent in oral and written English AND one or more of these languages: Portuguese, French, Spanish Ability to work within a team or across multiple teams (including remotely) as well as independently Values teamwork and collaboration, diversity a