medical writer

IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your spam folder. This is a fully remote position, open to candidates based in Belgium. Pay: $30–$60/hr Role Title: Medical Writer (Pharmaceutical) Role Type:...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

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 straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer...

We are seeking a Principal Medical Writer to support full Clinical Study Report (CSR) writing for Phase 1 , protocol development, and preparation of regulatory modules (2.7.1/2.7.2) . This role requires strong writing skills and attention to detail to ensure high-quality, inspection-ready deliverables.Key Responsibilities:Ensure all deliverables are...

Reading, Berkshire, United Kingdom Lisbon, Portugal Brussels, Brussels-Capital Region, Belgium Belgrade, Serbia Barcelona, Spain London, United Kingdom Madrid, Spain Full time R1571038 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...

IQVIA is seeking a Lead Medical Writer to act on a variety of writing projects and deliverables. You will prepare documents according to IQVIA SOPs and customer requirements, negotiate timelines, and mentor junior staff while ensuring quality and compliance.You will stay current with GCP and drug development knowledge, lead project work streams, and...

What we will accomplish together: Alsinova is looking on a regular basis for Medical Writers to join our consulting team for clients’ projects (from big pharma to small biotech) based in Belgium. Your mission (should you decide to accept it): Your potential challenges will be various, depending on the clients’ priorities. The list below gives you...

Alsinova in Belgium is seeking Medical Writers to join our consulting team for client projects across pharma and biotech. You will synthesize literature, draft, edit and update clinical development documents with high technical accuracy.The ideal candidate has at least 1 year of Medical Writing experience, strong English and French writing skills,...

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 straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

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...

RemoteJobsOne is seeking an experienced Medical Writer (Pharmaceutical) for a fully remote contractor role based in Belgium. You will contribute to AI-assisted clinical documentation and regulatory writing, shaping how models learn from high‑quality real‑world input and ensuring compliance with ICH guidelines.This high‑caliber position requires 5+...

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 updates, Biomarker Reports, and...

IQVIA seeks a Lead Medical Writer to act as the lead writer on a range of projects, ensuring documents align with SOPs and customer requirements within agreed timelines.The role involves senior review, negotiating timelines, and providing feedback to junior staff. You will stay current with GCP, drug development, and medical writing practices, collaborating...

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...

Syneos Health, Inc. is seeking a Principal I/II Medical Writer for fully remote work across Italy, UK, Spain, Poland or Ireland. The role focuses on regulatory submissions and clinical documentation support within our Clinical Solutions team.The position offers broad exposure to drug development programs and collaboration with cross-functional teams while...

We are seeking a Principal Medical Writer to support full Clinical Study Report (CSR) writing for Phase 1 , protocol development, and preparation of regulatory modules (2.7.1/2.7.2) . This role requires strong writing skills and attention to detail to ensure high-quality, inspection-ready deliverables.Key Responsibilities:Ensure all deliverables are...

IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your spam folder.This is a fully remote position, open to candidates based in Belgium.Pay: $30–$60/hrRole Title: Medical Writer (Pharmaceutical)Role Type: ContractorLocation:...

IQVIA is seeking a Principal Medical Writer to support full CSR writing for Phase 1 pharmacology studies, as well as protocol development and preparation of regulatory modules 2.7.1/2.7.2. This role requires meticulous writing and hands-on experience to deliver inspection-ready documents.You will manage document templates, coordinate QC, and collaborate with...

Johnson & Johnson Innovative Medicine is seeking a Medical Writer II, Regulatory Medical Writing to support across therapeutic areas. You will author regulatory documents, coordinate collaborative writing efforts, and ensure alignment with internal standards and regulatory guidelines.The role involves working in a hybrid setup (Beerse, Belgium or other...