Medical Writing and Regulatory Affairs Lead

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...

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 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...

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...

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: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...

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 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...

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...

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...

Barrington James is looking for a highly skilled professional to fill the role of Senior Manager Medical Writing and Regulatory Affairs. In this position, you will be responsible for managing the medical writing team, attending senior leadership pipeline meetings, and monitoring team performance. You will also provide regular updates to senior management on...

Become an integral part of Barrington James, a leading player in the clinical trials sector, as our new Medical Writing and Regulatory Director. In this role, you will be responsible for overseeing medical writing and regulatory submissions, ensuring compliance with all relevant regulations.About the Role:Lead a team of medical writers and regulatory...

About the RoleA leading Contract Research Organisation (CRO) specialising 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.With a competitive salary package of £70,000+ per annum, this senior-level position...

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...

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,...

Senior Medical Writing and Regulatory Submissions RoleWe are seeking an accomplished professional to lead our medical writing and regulatory teams. As the Head of Medical Writing and Regulatory Submissions, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables.This senior role involves strategic guidance on...

Job Title: Lead Medical Writer - Regulatory Affairs SpecialistEstimated Salary: £80,000 + Benefits (Central London)Company Overview:Cpl Life Sciences is a leading clinical research organisation dedicated to bringing innovation to patients globally. We're at the forefront of advancing medical knowledge and improving healthcare outcomes.Job Description:We're...

We are seeking a highly skilled Regulatory Affairs Lead to join our team at Warman O'Brien. This is an exceptional opportunity for a senior-level expert to lead our medical writing and regulatory activities, ensuring optimal resource allocation and driving business growth.Key Responsibilities:Accountable for all medical writing and regulatory tasks,...

Arevna is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials. We are currently seeking a Senior Regulatory Affairs Manager to lead our regulatory affairs team in Central London.Job Description:The successful candidate will be responsible for driving the development and commercialisation of our Medical Writing and...

Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. We are seeking an experienced medical writing and regulatory expert to join our team as Senior Director of Medical Content and Compliance.Key Responsibilities:Oversee the preparation and submission...