Offer summary

Qualifications:

Proficient in English grammar and sentence structure., 2 to 5 years of recent experience as a Medical Writer., Strong background in Clinical and/or Medical Devices., Knowledge of Medical Device Regulations (MDR) and experience in writing CER or PMSR reports..

Key responsibilities:

Perform literature searches and review scientific articles.

Summarize relevant information from research articles.

Coordinate with teams to collect and update project documents.

Ensure accuracy and completeness of clinical documents.

Job description

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.

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
Used to perform scientific literature searches in different databases
Experience in reviewing scientific literature
Understand about Medical Device Regulations (MDR)

Benefits