Regulatory Writing Expert

As a Regulatory Writing Expert at Life Sciences Recruitment, you will play a critical role in ensuring that our clients' products and services comply with regulatory requirements. Your expertise in regulatory affairs will help us navigate complex regulations and ensure that our content meets the highest standards of quality and accuracy. If you have a...

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...

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 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...

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...

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...

Barrington James, an esteemed clinical trials sector organisation, seeks a skilled Head of Medical Writing and Regulatory Operations to lead its medical writing team. This senior leadership position offers the chance to drive business growth and advance medical innovation.The ideal candidate will be responsible for overseeing the preparation and delivery of...

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...

Key ResponsibilitiesTaking full accountability of all medical writing and regulatory activitiesDirecting line management responsibilities for the Medical Writing team, with two employees under your managementProviding regulatory expertise to project teams on all aspects of the clinical trials processSupporting the organisation and preparation of regulatory...

About the RoleWe are looking for a highly skilled Head of Medical Writing and Regulatory Submissions to join our team at Barrington James. This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment.Responsibilities:Oversee the preparation and submission of study documentation, ensuring regulatory compliance and...

Job Title: Strategic Regulatory ExpertAt FD Technologies, we are seeking a skilled Strategic Regulatory Expert to join our Capital Markets Business in London. This is a perm role that requires strategic thinkers who thrive in fast-paced environments and possess strong experience with regulations such as EMIR/SFTR/IBOR/LIBOR/MIFIDII/BREXIT/FRTB.Key...