Role highlights
Full Time
Permanent
Mid
On-site
This mid-level Medical Writer position requires a candidate with a bachelor's degree and approximately moderate professional experience in medical writing or related fields. The role demands strong proficiency in creating clear, accurate, and well-structured medical documents, including clinical study reports, regulatory submissions, manuscripts, and educational materials. Candidates should have a solid understanding of medical terminology, clinical research processes, and regulatory guidelines such as ICH, FDA, or EMA standards. Attention to detail and the ability to interpret complex scientific data into accessible language for diverse audiences are essential. Experience collaborating with cross-functional teams including clinicians, researchers, and regulatory affairs professionals is important. The ideal candidate demonstrates excellent written communication skills, critical thinking, and the capability to manage multiple projects and meet tight deadlines. Familiarity with referencing software, document management systems, and adherence to ethical standards in medical communication will be advantageous. Overall, this role suits a professional with a foundational academic background in life sciences or related disciplines, combined with practical experience in medical writing, aiming to contribute to the development of high-quality scientific and regulatory documentation.
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