Senior Medical Writer—Lead Regulatory Submissions

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 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 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 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 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 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 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 life sciences provider is seeking a Senior Translation Project Manager to coordinate Regulatory Submissions translation projects. You will manage multiple projects, liaise with clients, and ensure high quality standards. Ideal candidates have over 4 years of project management experience in the language services industry, expertise in regulatory...