Regulatory Medical Writer

Job Title: Regulatory Medical WriterAbout MMS Holdings Inc.MMS Holdings Inc. is a leading Contract Research Organization (CRO) providing innovative data-focused services to the pharmaceutical, biotech, and medical device industries. Our scientific approach and technology-enabled services enable us to support complex trial data and regulatory submission...

Job SummaryWe are seeking an experienced Pre-Sales Solutions Architect Manager to join our team at Writer. In this role, you will be responsible for managing and mentoring a team of Solution Architects, each with extensive knowledge and experience in Data and AI technologies.ResponsibilitiesCreate proof-of-concept demonstrations and build strong...

Job Description:We are seeking a highly experienced Regulatory Medical Writer to join our team at TriloDocs, an innovative AI-powered software company based in London, UK. As a Regulatory Medical Writer, you will be responsible for developing and executing comprehensive training programs for end-users, conducting training sessions, and providing ongoing...

**About Actalent**We are a leading provider of expert talent to the pharmaceutical industry, and we are currently looking for a highly skilled Senior Medical Writer to join our UK team.The ideal candidate will have at least 3 years of experience in writing regulatory documents and have worked as the lead writer on multiple projects. They will be responsible...

Job Title: Lead Regulatory WriterBarrington James is seeking a highly skilled Lead Regulatory Writer to join our Medical Writing and Regulatory Affairs department. As a senior leader, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs.With a strong background in medical...

MMS Holdings Inc is a renowned CRO that provides innovative solutions to the pharmaceutical, biotech, and medical device industries.Job DescriptionWe are looking for a highly skilled Medical Content Writer - Regulatory Documents to create high-quality content for clinical development documents. The successful candidate will have a strong background in...

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...

Role and ResponsibilitiesRichmond Pharmacology is seeking a skilled Medical Writer to join our team in London Bridge. The successful candidate will have excellent written and verbal communication skills, with the ability to craft high-quality, scientifically accurate medical and scientific communications. You will be comfortable working independently and...

As a Medical Writer at Publicis Groupe, you will be responsible for translating complex scientific and clinical information into clear and concise documents.Job Description:We are seeking a Medical Writer with expertise in healthcare and pharmaceutical industries to join our team. The ideal candidate will have a strong understanding of regulatory guidelines...

Freelance Regulatory Writer JobBarrington James Limited is working with a Consultancy to find a talented Freelance Regulatory Writer.About the JobThis is a 12-month contract opportunity, offering flexible working hours and remote work arrangements. The ideal candidate will have a scientific academic background and at least 5 years of experience as a Medical...

About the RoleWe are seeking a highly skilled Regulatory Medical Writer Specialist to lead our clinical development programs. As a key member of our team, you will be responsible for overseeing medical writing staff and ensuring timely delivery of high-quality documents.ResponsibilitiesOversight of Medical Writing staff to ensure efficient document...

Job DescriptionBarrington James is seeking a Principal Medical Writer and Regulatory Compliance Specialist to join our team.The ideal candidate will have a strong background in medical writing and regulatory affairs, with a minimum of 5 years' experience in the industry.The salary for this role is estimated at £95,000 - £115,000 per annum, depending on...

Job Title: Medical WriterWe are seeking a highly skilled Medical Writer to join our team as a Danish specialist. The successful candidate will have expertise in healthcare and pharmaceutical industries, with a strong background in translating complex scientific and clinical information into clear and concise documents.Job Description:The primary...

Are you a skilled medical writer looking for a new challenge? We are seeking an experienced MEDICAL WRITER SPECIALIST to join our team at Worldwide Clinical Trials, a leading global contract research organization.We offer a competitive salary of €80,000 - €110,000 per year, depending on experience, plus benefits and opportunities for professional...

Medical Writing Lead Position OverviewWe are seeking a highly skilled and experienced Medical Writing Lead to join our team at Lifelancer.Job Description:As a Medical Writing Lead, you will be responsible for establishing strategies that drive clinical study and regulatory document authoring to the highest quality and regulatory standards. This is a hands-on...

Richmond Pharmacology is a leading Contract Research Organisation (CRO) that specialises in early-phase clinical trials for pharmaceutical and biotechnology sponsors.We offer a competitive salary of £55,000 - £70,000 per annum, depending on experience, as well as benefits such as private medical insurance, pension scheme, and 25 days annual leave plus bank...

Medical Content Translator and Writer Job DescriptionWe are looking for a Medical Writer with expertise in healthcare and pharmaceutical industries to join our team. The ideal candidate will be able to translate complex scientific and clinical information into clear and concise documents.Key Responsibilities:Clinical Writing: Prepare and edit clinical study...

Job SummaryWe are seeking a Principal Medical Writer to lead the development of high-quality regulatory documentation for our clients. This role will involve preparing documents for regulatory submissions, authoring client-specific documents, and project leadership.

Actalent is seeking a highly skilled Senior Medical Writer to join our team in the UK. As a key member of our clinical content team, you will play a vital role in producing high-quality regulatory documentation for the international pharmaceutical industry.With a strong background in medical writing and a deep understanding of regulatory requirements, you...

About the RoleWe are looking for a talented and ambitious SENIOR MEDICAL WRITER (full-time) with a strong background in scientific writing. This role offers an excellent opportunity to showcase your skills, enthusiasm, and creative thinking in developing compelling content for clients in the pharmaceutical industry. Based in Cheadle, Manchester, UK, this...