Regulatory Writing Expert

**Join Our Team as a Regulatory Writing Expert**MMS is seeking an experienced Regulatory Writing Expert to support our clinical development programs. As a key member of our team, you will have the opportunity to work on a variety of projects, from clinical protocols to clinical study reports.About the Role:In this role, you will be responsible for critically...

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...

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...

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...

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...

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...

Job OverviewVixio Regulatory Intelligence is seeking a highly skilled Regulatory Intelligence Expert to join our team.About UsWe are a leading provider of regulatory intelligence, helping clients navigate complex regulatory landscapes.We combine world-class content with advanced technology to deliver actionable insights and drive business success.The...

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...

As a Senior Regulatory Compliance Expert at Vixio Regulatory Intelligence, you will play a key role in shaping our company's technical compliance solution for online gaming operators and suppliers. This exciting opportunity allows you to leverage your expertise in regulatory requirements to design and develop a premium quality intelligence solution that...

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...

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...

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...

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...

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...

Key ResponsibilitiesPrepare high-quality documents per client specifications and regulatory authority guidelines.Lead authorship of complex documents, ensuring accuracy and adherence to regulatory requirements.Project leader - actively participate, develop, and write high-quality documents.You will also work closely with clients, internal teams, and partners...

Key Responsibilities:Critically evaluate and interpret medical literature to select primary resource materials for study design, statistical significance, scientific rigor, and absence of bias.Write and edit clinical development documents, including protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and...

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...

Job OpportunityBarrington James Limited is working with a Consultancy looking to expand their team.About the RoleWe are seeking an experienced Freelance Regulatory Writer, based in Europe, to join our client on a 12-month contract. This is a flexible FTE opportunity, allowing you to work remotely.5+ years of experience as a Medical WriterScientific academic...

Barrington James, a prominent organisation in the clinical trials sector, is seeking a seasoned Regulatory Expert Lead to spearhead medical writing and regulatory submissions. This role offers a unique opportunity to lead high-performing teams in a dynamic environment focused on advancing medical innovation.Key Responsibilities:Oversee the preparation and...

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...