Senior Medical Writer — Remote Spain

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead development of clinical study documents for global programs. Remote in Spain, candidate will plan, write, edit, format, and QC documents in accordance with regulatory guidelines and company style. The role requires 5+ years of senior medical writing experience,...

Athens, Greece Lisbon, Portugal Brussels, Brussels-Capital Region, Belgium Belgrade, Serbia Barcelona, Spain London, United Kingdom Madrid, Spain Full time R The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial...

We’re seeking an organized, motivated, and collaborative individual for our medical writing team. The senior medical writer will partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management in leading the planning and preparation of high-quality clinical regulatory documents....

Syneos Health is seeking a Senior Medical Writer with extensive clinical document writing experience (Protocols, CSRs and IBs) for a Functional Service Provider role. This remote opportunity supports global projects from Spain time zones.You will lead medical writing deliverables, coordinate reviews, and ensure regulatory compliance per ICH guidelines while...

Syneos Health is seeking a Senior Medical Writer with extensive clinical document writing experience (Protocols, CSRs and IBs) for a Functional Service Provider role. This remote opportunity supports global projects from Spain time zones. You will lead medical writing deliverables, coordinate reviews, and ensure regulatory compliance per ICH guidelines while...

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer for a remote role based in Spain. The candidate will lead development of clinical study documents, coordinate with sponsors and vendors, and ensure compliance with ICH, FDA, GCP and eCTD requirements. Experience includes planning, writing and editing protocols, CSRs, IBs,...

Ethos is seeking senior medical writers to help train AI models on professional documents, spreadsheets, and slide decks. You bring 5+ years in clinical research, biomedical science, or regulatory affairs and experience authoring or reviewing study reports and regulatory materials. This fully remote, flexible role offers 5-20 hours per week with ASAP start....

Senior Medical Writer/Principal Medical Writer Remote, Spain Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. Develops...

Senior Medical WriterThe Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International...