Medical Writing and Regulatory Director

Regulatory Affairs and Content StrategyAs the Medical Writing and Regulatory Affairs Director, you will be responsible for leading our medical writing team and developing strategic content initiatives to drive business growth.ResponsibilitiesDevelop and implement a content strategy that aligns with our business objectives.Collaborate with cross-functional...

We are seeking an experienced professional to lead our medical writing and regulatory teams. As a Senior Director, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and compliance with regulatory standards.Job Description:Manage the entire medical writing and regulatory...

We are looking for a seasoned professional to lead our Medical Writing and Regulatory Affairs department at Barrington James, a pioneering firm in the clinical trials sector. In this critical role, you will oversee the preparation and delivery of high-quality regulatory submissions and medical writing outputs.Job Details:This senior leadership position...

Role OverviewThis is a fantastic opportunity for a highly skilled professional looking to make a significant impact in the fields of medical writing and regulatory submissions. As the Head of Medical Writing and Regulatory, you will be responsible for leading and managing teams within a dynamic, research-driven environment dedicated to advancing medical...

Key ResponsibilitiesTaking full accountability of all medical writing and regulatory activitiesDirecting line management responsibilities for the Medical Writing team, with two employees under your managementProviding regulatory expertise to project teams on all aspects of the clinical trials processSupporting the organisation and preparation of regulatory...

Barrington James is a prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients. We are seeking a talented and experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing team in advancing medical innovation and supporting the development of...

About Richmond Pharmacology:We are 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.Location: London Bridge (Hybrid 4 Days...

Richmond Pharmacology, a leading Contract Research Organisation (CRO), is seeking an experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing and regulatory teams. As a senior leader, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and...

About the RoleBarrington James is a prominent organisation in the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients. We are seeking a highly experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing and regulatory submissions team.Job Summary:Lead the preparation and delivery...

Overview:Richmond Pharmacology, a leading Contract Research Organisation (CRO), is seeking an experienced Head of Medical Writing and Regulatory Submissions to lead and develop our medical writing and regulatory teams.Salary: Competitive Salary + Benefits (£80,000 - £100,000)About the Role:We are looking for a skilled professional to oversee the...

Job OverviewBarrington James is a leading clinical trials organisation seeking an experienced Medical Writing and Regulatory Lead. As a senior leader, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs.This role offers a unique opportunity to lead and manage teams within a...

Overview of the PositionBarrington James is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing team. As a senior leader, you will oversee the preparation and delivery of high-quality regulatory submissions and medical writing outputs, ensuring adherence to all relevant regulatory...

BioMarin Pharmaceutical Inc.Job OverviewThe estimated annual salary for this position is around $120,000 - $180,000 depending on location and experience. We are seeking a highly experienced Associate Director of Clinical Medical Writing to join our team. As a key member of the clinical development organization, you will be responsible for providing strategic...

Job SummaryWe are seeking a highly skilled and experienced Head of Medical Writing and Regulatory to lead our team in delivering high-quality regulatory submissions and medical writing outputs.The ideal candidate will have a strong background in medical writing and regulatory submissions, with experience in managing teams and ensuring compliance with...

Company OverviewArevna is a Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors.We are committed to advancing medical research and supporting the development of transformative therapies through excellence and innovation. Our team of experts works closely with clients to deliver...

Job Title: Medical Writing and Regulatory Submissions ExpertBarrington James, a leading organisation in the clinical trials sector, is seeking an experienced professional to fill this key role.Role Overview:This senior leadership position involves overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs,...

About Richmond PharmacologyWe are a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors.Job DescriptionWe are seeking an experienced Head of Medical Writing and Regulatory Affairs to lead and develop our medical writing and regulatory teams. The successful candidate will...

Job Description:We are seeking a skilled Medical Writing and Regulatory Affairs Lead to join our team at Be-IT Ltd in Central London. This is a hybrid role requiring you to be on-site 4 days a week.About the Role:The Head of Medical Writing and Regulatory Affairs will provide senior-level expertise and management for our client's medical writing team,...

Barrington James, an esteemed clinical trials sector organisation, seeks a skilled Head of Medical Writing and Regulatory Operations to lead its medical writing team. This senior leadership position offers the chance to drive business growth and advance medical innovation.The ideal candidate will be responsible for overseeing the preparation and delivery of...

About the RoleWe are seeking a Medical Writing and Regulatory Affairs Lead to join our dynamic team at Barrington James.In this role, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs, ensuring adherence to all relevant regulatory standards.The ideal candidate will have a...