Senior Regulatory Medical Writer — Remote

A leading biopharmaceutical solutions organization is seeking a Sr Regulatory Medical Writer to oversee and produce high-quality medical documents. This full-time remote role involves collaboration with clients and cross-department coordination to ensure regulatory compliance. The ideal candidate will have an advanced degree in life sciences, proven medical...

Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. We are agile and driven to accelerate the delivery of therapies, because we are passionate to...

A leading biopharmaceutical solutions organization in Madrid is seeking an experienced Senior Principal Medical Writer to develop regulatory documents for global submissions. In this role, you will manage writing projects, collaborate with cross-functional teams, and mentor junior writers. The ideal candidate has a strong background in regulatory writing...

**Company Description** Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere. We...

A leading global contract research organization is seeking an experienced Principal Medical Writer to develop high complexity clinical regulatory documents. This role requires a PhD or Master's degree, with a minimum of 6 years of eCTD submission writing experience. The ideal candidate will lead project teams, engage with stakeholders, and contribute to...

A leading global contract research organization is seeking an experienced Principal Medical Writer to develop high complexity clinical regulatory documents.¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible.This role requires a PhD or Master's degree, with a minimum of 6...

A global biopharmaceutical solutions organization is seeking a Principal Medical Writer to lead the completion of regulatory submission documents. This role requires 3-5 years of experience in medical writing, a strong understanding of regulatory standards, and excellent communication skills. Responsibilities include managing writing activities, producing...

**About this role** 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. Senior Medical Writer is part of the...

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to bringing the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training...

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to bringing the cancer treatments of the future to the patients of today. TRIO is seeking a Medical Writer to join our Medical Writing and Training...