Cross Border Talents is a global talent provider specializing in recruitment for the Engineering, ICT, and Multilingual sectors. Operating in over 102 countries, the company leverages a network of recruitment partners to offer permanent and talent leasing recruitment solutions. As a fully remote company, Cross Border Talents allows its team members to work from anywhere in the world, increasing diversity and providing cross-country opportunities. With a focus on customer experience, the company utilizes advanced technology and a user-friendly system to simplify the talent search process, ensuring privacy and security for its users.
Skills shortage • Staffing • Recruitment • Employment • engineering
February 8
Cross Border Talents is a global talent provider specializing in recruitment for the Engineering, ICT, and Multilingual sectors. Operating in over 102 countries, the company leverages a network of recruitment partners to offer permanent and talent leasing recruitment solutions. As a fully remote company, Cross Border Talents allows its team members to work from anywhere in the world, increasing diversity and providing cross-country opportunities. With a focus on customer experience, the company utilizes advanced technology and a user-friendly system to simplify the talent search process, ensuring privacy and security for its users.
Skills shortage • Staffing • Recruitment • Employment • engineering
• Cross Border Talents is searching for experienced Medical Writers focused on CER for our client in the Medical/Healthcare industry, with more than 85 years of history developing products and therapies found throughout hospitals and clinics. • As a Medical Writer, you will: • 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 • The tasks will be performed remotely.
• 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 • Used to perform scientific literature searches in different databases • Experience in reviewing scientific literature • Understand about Medical Device Regulations (MDR)
• 06 months contract, reneable • Fully remote work • Hourly payment • Flexible working hours
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