Senior Regulatory Medical Writer

A leading biopharmaceutical solutions organization is seeking a Senior Regulatory Medical Writer to lead the completion of pivotal medical writing deliverables. This remote role requires excellent communication skills and a strong understanding of regulatory standards. Responsibilities include generating clinical study reports, protocols, and other essential...

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...

A leading biopharmaceutical solutions organization is seeking a Sr Regulatory Medical Writer to oversee and produce high-quality medical documents.¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo.This full-time remote role involves collaboration with clients and...

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...

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...

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...

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...

Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor Updated: October 2, 2025 Location: Madrid, Spain Job ID: -OTHLOC-3529-2DMAD-2DR Description Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer...

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...