Medical Writer

The FTE Medical Writer willserve as an integratedmember ofthe team, deliveringmedical writing services for thedevelopment 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 updates, Biomarker Reports,andsubmission...

The FTE Medical Writer willserve as an integratedmember ofthe team, deliveringmedical writing services for thedevelopment 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 updates, Biomarker Reports,andsubmission...

IQVIA is seeking a full-time Medical Writer in Belgium to develop clinical documents including CT Reports, CT Protocols, IBs, and submission materials. The role emphasizes writing for eye health and inflammation, with senior-level experience preferred.You will embed in sponsor processes, manage timelines, and collaborate with cross-functional teams to ensure...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources...

Thermo Fisher Scientific is seeking a Senior Medical Writer to lead and deliver high‑quality publications, abstracts, and posters for peri‑ and post‑approval programs. This role emphasizes scientific accuracy, regulatory alignment, and clear communication in English, within a highly collaborative CRO environment.The ideal candidate has extensive...

IQVIA is seeking a highly experienced FTE Medical Writer to deliver clinical documents across CTRs, TDOs/CTPs, IBs and submission materials. You will embed within sponsor workflows and participate in planning, discussions, and training sessions while adapting to sponsor systems and templates.The role emphasizes writing quality, regulatory compliance, and...

Principal Medical Writer is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators’ Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization...

IQVIA seeks a Principal Medical Writer to lead the development of regulatory documents for global submissions, including IBs, CSRs, and MA submissions. You will guide cross-functional teams to ensure messages are data-driven, scientifically rigorous, and accurately presented.You will oversee multiple compounds, lead summary documents, and drive timely,...

Planet Pharma seeks a Clinical Editor in Belgium to join a fast-paced, globally recognized organization to ensure accuracy, consistency, and regulatory compliance of clinical documents.You will edit, fact-check, and collaborate with medical writers to prepare documents for inspection-readiness and regulatory review.The role emphasizes attention to detail,...