Medical Writer (CER)

EU citizen living in any country of EU or UK. Proficient in English grammar/sentence structure. Between 02 to 05 years of experience as Medical Writer (recent). Strong background in Clinical and/or Medical Devices. At least 02 years of experience in writing Clinical Evaluation Reports (CER) or Post-Market Surveillance Reports (PMSR). Good knowledge in drafting literature review and state of art documents. Good knowledge of MEDDEV Rev. 4 guidance. Used to perform scientific literature searches in different databases. Experience in reviewing scientific literature. Understand about Medical Device Regulations (MDR).

Perform scientific literature searches and collection of research articles from appropriate databases (e.g. PubMed and other search engines). Perform literature and database searches, reviews articles to extract relevant information, and summarizes information from identified articles. Demonstrate sound knowledge of the medical writing process, medical device regulations, and associated approval processes. Apply medical concepts and terminology appropriately. Update project-related tracking tools. Work with multiple teams to collect documents as required. Maintain records for all assigned projects, including archiving. Schedule and conducts document-related meetings, including the preparation of meeting agendas, key data points for discussion, and meeting minutes. Work closely with the study team to ensure that content and results in clinical documents are accurate and complete as required.