Medical Writing Director

Job OverviewWe are seeking a highly experienced Medical Writing Director to lead our clinical trials team. This role will be responsible for overseeing the preparation of high-quality regulatory submissions and medical writing deliverables.Key Responsibilities:Liaise with internal teams and external sponsors to ensure strategic advice and guidance on...

BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of...

About the RoleWe are seeking an experienced Senior Medical Writing Director to lead our medical writing activities for innovative Radiopharmaceuticals in Oxford, UK.This is a perfect opportunity for a Principal Medical Writer to step into an Associate Director position and take the lead on all medical writing activities.

Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This...

Head of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a...

Head of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a...

A leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation. HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON). MUST BE ABLE TO WORK IN THE UK...

A leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...

A leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...

About Richmond PharmacologyRichmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and contribute to the development of life-changing therapies.Job OverviewWe are...

Job Title: Senior Manager, Medical Writing – Regulatory AffairsJob Type: Permanent, full-time Location: Central London, UK – 4x a week in LondonRemuneration: Up to £80,000 + BenefitsAn exciting and rare opportunity for an experienced Medical Writer to join a growing clinical research organisation, which are at the forefront of bringing innovation to...

Job Title: Senior Manager, Medical Writing – Regulatory AffairsJob Type: Permanent, full-time Location: Central London, UK – 4x a week in LondonRemuneration: Up to £80,000 + BenefitsAn exciting and rare opportunity for an experienced Medical Writer to join a growing clinical research organisation, which are at the forefront of bringing innovation to...

Medpace is currently seeking an office or home based Director of Proposals to join our Clinical Operations team at our London office. The Director will collaborate closely with our medical experts and senior functional managers to create the operational strategy for new business development opportunities. This will include direct management of the proposal...

A prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions . This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...

A prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions. This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Description Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our...

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board.DescriptionWho We AreBioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.Since our founding in 1997, we have applied our scientific expertise...

A prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions. This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...

Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. ...

Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. ...