Regulatory Writing Lead

Company OverviewVivify Talent Limited is a small, agile regulatory writing consultancy that prides itself on providing top-tier services to clients across the UK.Estimated Salary£55,000 - £65,000 per annum based on experience and qualifications.Job DescriptionAs a Senior Regulatory Writer at Vivify Talent Limited, you will be responsible for leading the...

Job DescriptionA challenging role as a Medical Writing Lead is available in our organization, requiring expertise in regulatory writing and experience in managing cross-functional teams.Responsibilities:Regulatory Document Preparation: Prepare high-quality regulatory documents for NDA/MAA/IND submissions and briefing packages, adhering to regulatory...

Job Title: Head of Medical Writing and Regulatory SubmissionsTerm: Permanent, Full-timeSalary: Competitive Salary + Benefits (Private Medical, Private Dental, Pension, 33 days Annual leave (Inclusive of bank holidays & Many more)Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for...

Job Title: Head of Medical Writing and Regulatory SubmissionsA 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.Position Overview:We are hiring a...

Richmond 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.The Role:We are seeking an experienced and...

Unlock Your Potential as a Senior Medical Writing Lead at Barrington JamesWe are seeking an accomplished Senior Medical Writing Lead to join our dynamic team at Barrington James. This exciting opportunity offers the chance to lead and manage teams within a fast-paced, research-driven environment dedicated to advancing medical innovation.About the Role:As...

About VixioVixio is a leading Regulatory Technology (RegTech) platform that helps businesses navigate the complexities of regulatory compliance in the payments and gambling industries.

Job Summary:We are seeking a highly experienced and accomplished Head of Medical Writing and Regulatory Submissions to lead and develop our medical writing and regulatory teams.As a senior leader, you will play a pivotal part in overseeing the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and...

Job OverviewWe are seeking an experienced and accomplished Head of Medical Writing and Regulatory Submissions to lead and develop our medical writing and regulatory teams.

Established chemical regulatory science consultancy is seeking a delivery-focused Regulatory Affairs Specialist to cover an increasing workload.This role will take the lead on physical/chemical properties/analytical methods and method validation for plant protection products. Key responsibilities include:Providing clients with regulatory advice on substance...

Job DescriptionThis Senior CMC Regulatory Document Specialist role is responsible for preparing and submitting high-quality CMC regulatory documents to support registration activities for both small molecule and biopharmaceutical therapeutic assets.ResponsibilitiesPrepare, review, and finalize regulatory submission documents for late-stage clinical...

A leading Contract Research Organisation (CRO) specialising in early-phase clinical trials seeks a highly skilled professional to lead their medical writing and regulatory teams. With a focus on excellence and innovation, the company is looking for an experienced Head of Medical Writing and Regulatory Submissions to drive successful project outcomes.Key...

Role Overview:Barrington James is seeking an exceptional Senior Medical Writing and Regulatory Submissions Specialist to lead our Medical Writing and Regulatory Affairs department. As a key member of our team, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs, ensuring...

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...

Role OverviewA challenging opportunity has arisen for a Regulatory Affairs Strategist to join VRS Regulatory's team. About the RoleWe are seeking an experienced Regulatory Affairs Strategist to develop and implement regulatory strategies for plant protection products in specific geographical territories. Develop and execute regulatory strategies for product...

Role OverviewVixio Regulatory Intelligence is seeking a highly skilled Regulatory Compliance Expert to lead the development of a premium technical compliance solution.The ideal candidate will have experience in compliance roles at regulated gambling operators or technology providers and possess strong communication skills.

Associate Director, Medical WritingJob Type: PermanentLocation: Oxford, UK – Hybrid/RemoteRemuneration: Attractive salary and packageAn exciting opportunity for an experienced Medical Writer to join a growing biotechnology company who are at the forefront of Oncology innovation within Radiopharmaceuticals.As an Associate Director, Medical Writing, you will...

Job Title: Associate Director, Medical WritingJob Type: Permanent, full-timeLocation: Oxford, UK – Hybrid/RemoteRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Medical Writer to join our growing biotechnology company, at the forefront of Oncology innovation within Radiopharmaceuticals.Job Responsibilities:Lead the...

Job OverviewWe are looking for a skilled Medical Writer to join our team. As a Danish specialist, you will have expertise in healthcare and pharmaceutical industries, with a strong background in translating complex scientific and clinical information into clear and concise documents.Key Responsibilities:The primary responsibility of this role is to...

Job Summary:The British Veterinary Association is seeking a highly skilled and experienced Head of Pharmacovigilance to join their team. In this exciting role, you will be responsible for the post-authorisation surveillance of veterinary medicines through the collation of suspected adverse event reports among other mechanisms.Key Responsibilities:Develop and...