Regulatory Submissions Jobs in UK

Closing Date23/02/2026JobTitle:Area Risk SpecialistLocation:Hampshire area- you can be based at our offices located in Chichester/ Budds Farm- Hybrid (3 days office/ site remaining WFH)- Driving licence essential due to site visit requirementsContractType:PermanentHours:37Salary: Up to 48000 per ann...

You will lead medical writing activities that support clinical development and regulatory submissions. You will work closely with clinical pharmacology non-clinical pre-clinical research regulatory biostatistics and/or external partners to plan author and deliver complex documents. We value clear sc...

Join IQVIA on our mission to accelerate innovation for a healthier world!We are seeking Senior Clinical Research Associates across the UK to strengthen our cFSP sponsor-dedicated team.Why IQVIAWe share a passion for the work we do and the impact it has on customers and patients.We are innovative cur...

Make your mark for patientsAre you passionate about advancing patient safety and drug development Join ourPatient Benefit Risk and Medical Safety teamas aBenefit Risk Lead where your analytical mindset and collaborative and proactive attitude will help deliver safe and effective treatments. This ro...

London 23 days onsite (hybrid)Are you a regulatoryfocused Study StartUp expert who thrives on ownership and compliance Were looking for a Study StartUp PM to lead countrylevel submissions approvals and site readiness for a global clientdedicated program.What youll ownOversight of endtoend regulato...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

We are seeking talented individuals across all levelsfrom Graduate to Technical Directorto join our Environment EIA & Consents team. Working within a collaborative multi-disciplinary environment you will contribute to high-quality environmental assessments planning strategies and regulatory submissi...

We are seeking a Software Engineer to join our Regulatory Reporting team. This role focuses on building and operating reliable auditable and deterministic backend systems that support regulatory reporting across multiple jurisdictions. You will work closely with Staff Engineers the Engineering Manag...

How you will contribute  During the two years you will spend time in different focus areas of the Legal tribe which means youll have exposure to a wide range of legal matters spanning across multiple parts of the business. From day one youll be working alongside lawyers within the Legal team in Lond...

Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to...

A Bit About UsWere Doccla and were redefining where and how healthcare is delivered.Our Virtual Ward and Remote Monitoring Solutions enable hospitals and health systems to care for patients at home. We support patients across the full care journeyfrom early discharge and acute recovery to long-term...

Title:Head of Regulatory Submission Project ManagementCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Medical Writer - Make an Impact at the Forefront of InnovationThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts...

Title:Microbiology Team LeaderCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global h...

Title:MS&T Principal Analytical ScientistCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience wi...

We create a place where people can grow be their best be safe and feel welcome valued and included. We offer a competitive salary an annual bonus based on company performance healthcare and wellbeing programmes pension plan membership and shares and savings programme.We embrace modern work practises...

Associate Director Chemical Developer Location: MacclesfieldCompetitive salary and Benefits Hybrid working 3 days a week in the office About us: At AstraZeneca were united by a bold ambition: to push the boundaries of science and deliver life-changing medicines to patients worldwide. As a global sci...

About UsSharkNinjais a global product design and technology company with a diversified portfolio of 5-star rated lifestyle solutions that positivelyimpactpeoples lives in homes around the world. Powered by two trusted global brands Shark and Ninja the company has a proventrack recordof bringing disr...

Title:Senior Medical WriterCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs...

Title:Qualified PersonCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs in t...