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Experience Level
Experience
Qualifications
To be successful in this role, you should meet the following qualifications:EU citizenship with residency in any EU country or the UK.Excellent command of English grammar and sentence structure.A minimum of 2 to 5 years of recent experience as a Medical Writer.A strong background in Clinical and/or Medical Devices.At least 2 years of experience in drafting Clinical Evaluation Reports (CER) or Post-Market Surveillance Reports (PMSR).Proficient in conducting literature reviews and creating state-of-the-art documents.Familiarity with MEDDEV Rev. 4 guidance.Experience in performing scientific literature searches across various databases.A solid understanding of Medical Device Regulations (MDR).
About the job
Join Cross Border Talents as we seek skilled Medical Writers with expertise in Clinical Evaluation Reports (CER) to support our esteemed client in the Medical and Healthcare sector. With over 85 years of experience, our client has a rich history of developing innovative products and therapies that are vital in hospitals and clinics worldwide.
In your role as a Medical Writer, you will be responsible for:
Conducting thorough scientific literature searches and gathering research articles from relevant databases such as PubMed and other platforms.
Reviewing literature to extract and summarize pertinent information from selected articles.
Demonstrating a comprehensive understanding of the medical writing process, medical device regulations, and related approval workflows.
Utilizing medical terminology and concepts accurately and effectively.
Updating and maintaining project-related tracking tools.
Collaborating with various teams to compile necessary documentation.
Keeping detailed records for all assigned projects, including archiving processes.
Coordinating document-related meetings, preparing agendas, key discussion points, and minutes.
Working closely with the study team to ensure that clinical documents accurately reflect content and results.
This position is fully remote, allowing you to work from anywhere.
About Cross Border Talents
Cross Border Talents is a dynamic recruitment agency dedicated to connecting talented individuals with leading companies in the Medical and Healthcare sectors. Our client’s legacy spans over eight decades, during which they have continuously innovated and contributed to the betterment of healthcare services globally.
Medical Writer specializing in Clinical Evaluation Reports
Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.
Unlock Your Potential
Generate Job-Optimized Resume
One Click And Our AI Optimizes Your Resume to Match The Job Description.
Is Your Resume Optimized For This Role?
Find Out If You're Highlighting The Right Skills And Fix What's Missing
Experience Level
Experience
Qualifications
To be successful in this role, you should meet the following qualifications:EU citizenship with residency in any EU country or the UK.Excellent command of English grammar and sentence structure.A minimum of 2 to 5 years of recent experience as a Medical Writer.A strong background in Clinical and/or Medical Devices.At least 2 years of experience in drafting Clinical Evaluation Reports (CER) or Post-Market Surveillance Reports (PMSR).Proficient in conducting literature reviews and creating state-of-the-art documents.Familiarity with MEDDEV Rev. 4 guidance.Experience in performing scientific literature searches across various databases.A solid understanding of Medical Device Regulations (MDR).
About the job
Join Cross Border Talents as we seek skilled Medical Writers with expertise in Clinical Evaluation Reports (CER) to support our esteemed client in the Medical and Healthcare sector. With over 85 years of experience, our client has a rich history of developing innovative products and therapies that are vital in hospitals and clinics worldwide.
In your role as a Medical Writer, you will be responsible for:
Conducting thorough scientific literature searches and gathering research articles from relevant databases such as PubMed and other platforms.
Reviewing literature to extract and summarize pertinent information from selected articles.
Demonstrating a comprehensive understanding of the medical writing process, medical device regulations, and related approval workflows.
Utilizing medical terminology and concepts accurately and effectively.
Updating and maintaining project-related tracking tools.
Collaborating with various teams to compile necessary documentation.
Keeping detailed records for all assigned projects, including archiving processes.
Coordinating document-related meetings, preparing agendas, key discussion points, and minutes.
Working closely with the study team to ensure that clinical documents accurately reflect content and results.
This position is fully remote, allowing you to work from anywhere.
About Cross Border Talents
Cross Border Talents is a dynamic recruitment agency dedicated to connecting talented individuals with leading companies in the Medical and Healthcare sectors. Our client’s legacy spans over eight decades, during which they have continuously innovated and contributed to the betterment of healthcare services globally.