Senior Clinical Regulatory Writer

Med Communications International is seeking a Regulatory Writing Specialist (Clinical) with 3+ years of hands-on pharmaceutical regulatory writing experience. The role involves authoring CSRs, clinical protocols, IBs, and CTD Module 2 documents, plus coordinating client-facing projects and QC reviews. The position supports regulatory submissions...

Decskill, founded in 2014 as an IT Consulting Company, places paramount importance on its greatest asset: its people. Our main mission is to deliver value through knowledge and talent, and we achieve this by fostering a culture of excellence and investing in the development and well‑being of our people. With over 600 dedicated professionals and offices in...

Syneos Health is seeking a Senior Medical Writer with strong expertise in clinical document writing, including protocols, CSRs and IBs. This role focuses on delivering high-quality manuscripts and regulatory submissions while guiding a team of writers and collaborating with cross-functional teams. The position offers remote work with potential EST/CST...

Regulatory Writing Specialist (Clinical) About the job Regulatory Writing Specialist (Clinical) Senior Regulatory Writing Specialist Clinical & Nonclinical | Pharmaceutical Industry About the Role We are seeking a Regulatory Writing Specialist with at least 3 years of hands-on pharmaceutical regulatory writing experience, particularly in clinical...

Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs) Updated: September 22, 2026 Location: Remote, 1, Portugal Job ID:25112637-OTHLOC-3540-2DR Description Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs) Syneos Health® is a leading fully-integrated life sciences services...

Syneos Health, Inc. is seeking a Senior Medical Writer for Europe, home-based within our FSP Team.The role involves leading medical writing deliverables across studies, coordinating with data management, biostatistics, regulatory affairs, and medical affairs to ensure high-quality submissions. Ideal candidates have 3–5 years of medical writing experience,...

Regulatory Writing Specialist (Clinical) About the job Regulatory Writing Specialist (Clinical) Senior Regulatory Writing Specialist Clinical & Nonclinical | Pharmaceutical Industry About the Role We are seeking a Regulatory Writing Specialist with at least 3 years of hands-on pharmaceutical regulatory writing experience, particularly in clinical...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

Alignerr is seeking a Principal Clinical Scientist to shape AI training using regulatory-grade clinical data. This fully remote, hourly-contract role demands senior expertise in trial design and regulatory science to ensure AI systems are built on scientifically sound data for biomedical research. You will design protocols, audit results, and evaluate...