medical writer

Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad...

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...

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...

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,...

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...

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...

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...

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 submission...

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 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,...

Akkodis is seeking an experienced Medical Writer to join their team in Belgium. The role involves medical writing and quality checking, focusing on price and reimbursement files for authorities and supportingValue and Patient Access Managers and other writers.Applicants should have at least 3 years in medical writing, strong French writing skills, and...

IQVIA Inc is seeking a Principal Medical Writer responsible for developing regulatory documents for submissions to authorities worldwide. You will guide cross-functional teams, oversee multiple compounds, and ensure high-quality, data-driven clinical messages across IBs, CSRs, and submission documents.You will lead writing efforts, provide direction to other...

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 examples...

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 submission...

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...

IQVIA is seeking a Principal Medical Writer to lead the development of regulatory documents for global submissions. You will guide cross-functional teams, ensuring scientifically rigorous, data-accurate, and well-presented documents such as IBs, CSRs, and submission dossiers.You will oversee the writing of summary documents, manage timelines, and contribute...

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...

IQVIA is seeking an FTE Medical Writer to deliver writing services for CTRs, protocols, IBs and submission documents, with emphasis on eye health and inflammation. You will work embedded in sponsor processes, manage timelines, and contribute to cross‑functional team discussions.The role requires about five years of medical writing experience in biopharma...