Remote 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. 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 global biopharmaceutical organization is seeking a Senior Principal Medical Writer in Barcelona, Spain. In this role, you will develop regulatory documents for submission to agencies and manage medical writing projects. You will work closely with cross-functional teams and mentor junior staff. The position requires strong project management skills and...

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 leading biopharmaceutical solutions organization is seeking a remote Senior Medical Writer to lead the completion of medical writing deliverables. This role requires 3-5 years of relevant experience in science or medical writing, especially within the biopharmaceutical industry. The ideal candidate will possess a strong understanding of FDA and ICH...

**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...