Regulatory Medical Content Lead

Vivify Talent is looking for a Regulatory Content Lead to support the development of our specialty pharmaceutical products. As a key member of our clinical and regulatory team, you will be responsible for creating high-quality clinical documents, including Clinical Trial Applications and Investigational Medicinal Product Dossiers.This is a home-based role...

About Vivify Talent LimitedWe are a specialty pharmaceutical company dedicated to delivering innovative solutions to patients and healthcare professionals. Our team is passionate about creating high-quality content that meets regulatory requirements and improves patient outcomes.Job SummaryWe are seeking a Principal Medical Writer to join our team as our...

Job SummaryWe are a specialty pharmaceutical company looking for a Principal Medical Writer to join our team as our first Medical Writer and partner closely with clinical and regulatory teams. This role can be home based anywhere.About UsWe are a specialty pharmaceutical company with a strong focus on innovation and customer...

About the RoleWe are a specialty pharmaceutical company looking for a Principal Medical Writer to join our team. This role involves working closely with clinical and regulatory teams to develop a broad range of clinical documents.Job OverviewVivify Talent Limited is a dynamic company that values innovation and collaboration. As our first Medical Writer, you...

About the PositionThis is a fully remote role that offers flexibility and autonomy. As our first Medical Writer, you will be responsible for developing high-quality content that meets regulatory requirements and supports our mission to deliver innovative solutions to patients and healthcare professionals.Responsibilities and ExpectationsDeveloping clinical...

Job OpportunityWe are offering a unique opportunity for an experienced Medical Writer to join our team as a Principal Medical Writer. This role will involve creating high-quality medical content and partnering closely with clinical and regulatory teams.About Vivify Talent LimitedWe are a leading provider of talent solutions to the pharmaceutical industry....

Job DescriptionCpl Life Sciences is an established IVD manufacturer seeking a highly skilled Regulatory Affairs Officer to manage product licenses and ensure compliance with international regulations. This role offers an exciting opportunity to join a growing department and support our growth as a leading company in the life sciences industry.Main...

About the JobWe are recruiting for a Medical Devices Regulatory Expert to join our team in Edinburgh. As a key member of our Regulatory Affairs & Quality team, you will be responsible for ensuring compliance with international regulations and standards for medical devices.Key ResponsibilitiesDevelop and implement regulatory strategies for medical...

About UsWe are a dynamic global health innovation company that uses technology, data, and creativity to make a meaningful impact on the world.As a Medical Writer, you will be part of our innovative team that brings together healthcare, marketing and communications, tech, and people. You will have the opportunity to use your skills to create engaging content...

Job DescriptionFully Remote OpportunityJob SummaryWe are seeking a highly experienced Principal Regulatory Writer to join our team as our first Medical Writer and collaborate closely with clinical and regulatory teams. The ideal candidate would have worked with a broad range of clinical documents, ensuring compliance and quality in regulatory submissions....

Cpl Life Sciences is seeking a talented Medical Device Regulatory Coordinator to join our team. This role is based in the outskirts of Edinburgh, Scotland, UK, with 3x a week on-site requirement, offering an estimated salary of £35,000 to £40,000 + benefits.As a Medical Device Regulatory Coordinator, you will be responsible for managing product license...

**About the Role:** We are seeking a highly skilled Medical Device Compliance Officer to join our Regulatory Affairs Department. In this role, you will be responsible for ensuring the compliance of our medical devices with global regulatory requirements.**Key Responsibilities:Preparing and compiling regulatory documentation in compliance with ISO13485, IVD...

Regulatory Affairs Job OpportunityCpl Life Sciences is seeking a Global Regulatory Lead to join our team in Edinburgh, Scotland. This is a full-time, permanent position requiring 3x weekly on-site presence.Salary: £45,000 per annum.The successful candidate will be responsible for managing product license registration with global regulatory authorities,...

We are seeking a highly experienced Global Regulatory Affairs Lead to join our team at IQVIA. The successful candidate will have a strong background in pharmaceutical governance and regulatory compliance.The ideal candidate has 10+ years of experience in the clinical trial or medical device domain, with a deep understanding of current global regulatory...

Job Description: We are seeking a highly skilled and experienced professional to lead our global market access team as a Director, Data Quality. This role requires strong leadership and collaboration skills, as well as expertise in scientific and medical writing. The ideal candidate will have a background in clinical, life sciences, or a related scientific...

Job DescriptionWe are looking for an experienced Digital Content Manager to lead the development of our digital content program. The successful candidate will have a strong understanding of digital content strategy and experience managing a team.The role will involve implementing a Content Strategy that meets key milestones and objectives in support of...

Lloyds Banking Group is seeking a Content Strategy Lead to help us shape the future of banking.As a key member of our team, you will lead the development of our content strategy, combining research and insights with clear people-focussed language to refine and develop conversations with customers to help them do what they need to do.With a strong background...

SRG, a leading Biotechnology company based in Edinburgh, is seeking a Senior Regulatory Compliance Officer to join their team on a permanent basis. The estimated salary for this role is £55,000-£65,000 per annum.About the RoleThe Senior Regulatory Officer will be responsible for delivering end-to-end regulatory packages under ODM-Distributor schemes in...

Company Overview: SRG is a leading Biotechnology company based in Edinburgh, Scotland. We are seeking an experienced Regulatory Affairs Officer to join our team on a permanent basis.Salary: £55,000 - £65,000 per annum depending on experience.Job Description:We are looking for a skilled Regulatory Affairs Officer to build regulatory strategy, determine...

Job DescriptionAs a Regulatory Operations Lead, you will be responsible for managing and overseeing the end-to-end onboarding process for ICS clients. This includes reviewing Client Due Diligence (CDD) documentation to ensure compliance with regulatory standards.You will also prepare and present business acceptance forms, chair business acceptance meetings,...