This is a remote position for a Senior Medical Information Writer that involves developing core medical information deliverables, including SRDs, FAQs, Custom Response Documents, and interactive SRDs. Candidate should independently manage assignments and consistently deliver high-quality, scientifically accurate content with minimal supervision. This role can be based in the UK, Ireland, Spain, Italy, Poland, Germany or Portugal.
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As a Sr. Medical Writer, you will develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and AMA Medical Writing styles. You will actively participate in study and/or project team meetings to provide input regarding medical writing deliverables, timelines and any processes needed for the completion of regulatory documents. Assist in working practices to allow the effective and efficient preparation of quality documents.