Medical Writer (CER)

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Requirements:

• 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).

Responsibilities:

• 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.