Overview Senior Medical Writer (FSP) to lead and deliver clear, compliant medical writing for protocols, CSRs, IBs and related documents. You will coordinate across departments, mentor junior writers, and ensure high-quality deliverables wi...Read More>>.

Overview As Principal I/II Medical Writer, you will lead regulatory submission activities within a fully remote role across Europe. You’ll work within Syneos Health’s Clinical Solutions, applying deep medical writing expertise to suppor...Read More>>.

A leading healthcare communications agency in Manchester is seeking an Analyst / Medical Writer. The role involves analyzing clinical trial data and creating various communication materials for clients. Successful candidates will have a degree in a s...Read More>>.

Senior Manager, Regulatory Medical WritingSenior Manager, Regulatory Medical WritingGet AI-powered advice on this job and more exclusive features.Direct message the job poster from Cpl Life SciencesManaging Consult...Read More>>.

A global medical communications company is looking for a Medical Writer in Edinburgh. You will analyze clinical trial data and create materials for diverse audiences while collaborating closely with clients. This full-time role offers a starting sala...Read More>>.

A leading health communications agency in Greater London is seeking an Associate Director to lead a writing team focused on scientific content and medical communications. The role involves client interaction and strategy development, requiring signif...Read More>>.

Ergomed Group seeks a Senior Director / Executive Director Medical Writing to lead the PV Medical Writing function, ensuring high‑quality, compliant, and timely deliverables while building a capable team.You will drive regulatory strategy...Read More>>.

Agomab seeks a Sr. Director of Medical Writing to anchor our hybrid medical writing function. You will own narrative strategy, document quality, and CRO relationships across clinical programs, including regulatory submissions. Lead AI-enabled tool...Read More>>.

Description This is a newly created position and a foundational hire for Agomab's Medical Writing function. The Sr. Director, Medical Writing will serve as the anchor of our hybrid medical writing model — working embedded across all...Read More>>.

Madano is seeking a Senior Medical Writer to deliver scientifically robust content across medical communications, including clinical publications and medical affairs. You will lead on account workstreams, mentor junior writers, and collaborate wit...Read More>>.

Ethos is seeking senior medical writers with 5+ years in clinical research, biomedical science, or pharmaceutical/regulatory affairs to train our latest language model on professional documents, spreadsheets, and slide decks. The role is fully rem...Read More>>.

MMS Holdings Inc. in Greater London is seeking a Senior Regulatory/Medical Writing Lead to shape regulatory documentation strategies and ensure high-quality submissions.You will mentor Medical Writing staff, manage complex projects end-to-e...Read More>>.

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great...Read More>>.

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great...Read More>>.

MMS is a data-focused clinical research organization seeking an experienced Medical Writing Lead in the UK. You will oversee regulatory writing activities, mentor colleagues, and ensure high-quality deliverables across trials and submissions....Read More>>.

Manager Regulatory Medical Writing XTA Johnson and Johnson•High Wycombe, GB At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented,...Read More>>.

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high‑quality clinical study documents in line with regulatory guidelines. You will plan, write, edit, format, and QC key documents, e...Read More>>.

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead development of critical clinical study documents remotely in the United Kingdom. This role requires writing, editing, and QC across protocols, IBs, CSRs a...Read More>>.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to...Read More>>.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to...Read More>>.

MMS is an award-winning, data-focused clinical research organization in the UK seeking a Senior Medical Writer to lead regulatory writing and mentor a team of Medical Writing professionals.You will ensure quality and compliance across deliv...Read More>>.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to...Read More>>.

Roche Diagnostics Solutions (RDS) seeks a Clinical Development Lead within the CEI team to drive documentation for clinical studies, reports and regulatory submissions. You will collaborate with SMEs across CDMA and other functions to support new...Read More>>.

Mantra Systems Ltd in the UK is seeking a full-time regulatory writer to join our core team in Sheffield. You will contribute to literature reviews, Clinical Evaluation submissions, and the preparation of technical files under EU MDR, IVDR and FDA...Read More>>.

MMS, a data-focused clinical research organization, invites you to join a collaborative, innovative team in Belfast. The role focuses on regulatory and medical writing leadership, mentoring others, and guiding complex trial documentation and regul...Read More>>.

Fortrea is seeking a Regulatory Medical Writer II to own high-complexity Phase II‑IV clinical regulatory documents and manage lifecycle from planning to final delivery, closely coordinating with cross‑functional teams. You will author protocol...Read More>>.

MMS Holdings Inc. is seeking an experienced Medical Writer to join our regulatory documentation team. You will ensure compliance with CFR Part 11, FDA, GCP; mentor junior staff; lead complex writing projects from start to finish.The role re...Read More>>.

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great...Read More>>.

Johnson & Johnson is seeking a Manager, Regulatory Medical Writing to support across key therapeutic areas within our Integrated Data Analytics & Reporting (IDAR) business. Hybrid work with optional international postings and case-by-case remote p...Read More>>.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are p...Read More>>.

Business Support Secretary12-Month Fixed Term ContractWe are recruiting for an experienced Business Support Secretary to join a successful organisation on a 12-month fixed-term contract. This is an excellent opportunity for...Read More>>.

Version 1 is a global technology services company, delivering impactful change to help our customers Version 1 has celebrated 30 years in Technology Services and continues to be trusted by global brands to deliver solutions that drive customer...Read More>>.

Technical Author / Technical WriterLocation: County DownJob Type: Full-time, PermanentIndustry: Engineering / ManufacturingWhat's in it for you?...Read More>>.

About the RoleAn exciting opportunity has arisen for an experienced Bid Writer to join an established and award-winning construction and civil engineering organisation.The business delivers a diverse po...Read More>>.

Excel Recruitment is delighted to be recruiting for a Bid Writer on a permanent full-time basis in Dungannon with a starting salary of £45,000 depending on ex...Read More>>.

MCS Group are delighted to be partnering with an award-winning construction company to recruit a motivated Bid Writer. This is a fantastic opportunity to join a well-established bid team, playing a key role in the continued success of the busin...Read More>>.

VANRATH is recruiting a Bid Writer/Manager for a well-established engineering company based in Northern Ireland. This is a senior role leading complex bids and tenders while driving business development activity in support of...Read More>>.

Honeycomb is delighted to be recruiting for a Legal Secretary on behalf of a well-established and highly regarded law firm in East Belfast, offering an excellent opportunity to join a busy legal team supporting a varied matrimonial and family l...Read More>>.

Your New CompanyA prominent UK law firm with offices in Belfast are seeking a highly organised and proactive Litigation Secretary to provide comprehensive secretarial and administrative support to their Defence Litigation Depa...Read More>>.

Your new company Hays are working exclusively with The Pharmaceutical Society NI to recruit for a Secretary to the Statutory Pharmaceutical Society NI is the statutory regulatory body for pharmacists and p...Read More>>.

Litigation Secretary Belfast | Competitive Salary + Benefits | PermanentYour new companyHays are delighted to be recruiting on behalf of a highly regarded Belfast law firm with a...Read More>>.

Personal Secretary required to work with our client the Belfast Trust, this role will be based at the Knockbracken Health Care Park Belfast. Hours of work are Monday to Friday 9am - 5pm with an hourly pay rate of £14.06, this...Read More>>.

Litigation Secretary Full TimeLocation: Shankill Road, BelfastHours: MondayFriday, 9:00am5:00pmSalary: Competitive, dependent on experienceWe are current...Read More>>.