Remote Medical Writer

Summary

The job involves performing scientific literature searches and writing Clinical Evaluation Reports (CER) or Post-Market Surveillance Reports (PMSR). The candidate should have at least 2 years of experience in this field, be proficient in English grammar/sentence structure, and have knowledge of MEDDEV Rev. 4 guidance and Medical Device Regulations (MDR).

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 knownledge in drafting literature review and state of art documents
• Good knowledge of MEDDEV Rev. 4 guidance
• Experience in reviewing scientific literature
• Understand about Medical Device Regulations (MDR)

Responsibilities

• Perform scientific literature searches and collection of research articles from the 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

Benefits

• 6 months contract, renewable
• Fully remote work
• Hourly payment
• Flexible working hours