Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
Job Overview Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of
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 Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB
We are looking for experienced Freelance Medical Writers to support an immediate requirement with a leading international organisation working within the life sciences industry. This opportunity would suit an experienced clinical/regulatory writer who has current availability to take
Overview Cactus Life Sciences partners with global biopharma to drive innovation and improve patient outcomes through agile, science-driven medical communications — transforming complex data into actionable insights. Please note: We are a remote-first organization, and we
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical
IQVIA in Frankfurt/Main is seeking an FTE Medical Writer to deliver high-quality clinical documents for regulatory submissions, including CTRs, IBs, and CTP amendments, with a focus on eye health and inflammation. The FTE Medical Writer will work embedded in
Frankfurt/Main, Germany | Full time | Hybrid | 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
Reading, Berkshire, United Kingdom Lisbon, Portugal Brussels, Brussels-Capital Region, Belgium Belgrade, Serbia Barcelona, Spain London, United Kingdom Madrid, Spain Full time R Job Overview Acts as Lead Medical Writer on most types of writing projects. Prepares assigned
Medical Writer II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at