Reading, England, United Kingdom · Hybrid
The Clinical Trials Assistant will play a vital role in supporting Local Trial Managers and Clinical Research Associates. Key deliverables include tracking progress of the clinical trial, managing study data, budget, inv…
Skills: Clinical Trial Tracking, Study Data Management, Trial Master File Maintenance, GCP, ICH Guidelines
Reading, England, United Kingdom · Hybrid
Director Regulatory Affairs ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integ…
Skills: Regulatory Strategy, Submission Management, European Regulatory Procedures, Stakeholder Management, Agency Negotiation
London, England, United Kingdom · Remote OK
$34k–$61k/yr
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requiremen…
Skills: Site Activation, Regulatory Submissions, GCP/ICH Guidelines, Clinical Research, Contract Management
Reading, England, United Kingdom · On-site
Job Location READING TECH CENTER Job Description Ready to fuel the success of globally renowned brands that millions of consumers can’t live without? Ready for career where you are fully supported by world-class training…
Skills: Strategic Thinking, Business Acumen, Scientific Data Evaluation, KOL Management, Medical Strategy Execution
Reading, England, United Kingdom · Hybrid
Clinical Trial Administrator - UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation,…
Skills: Clinical Trial Coordination, Clinical Trial Documentation, Regulatory Compliance, Study File Management, Cross-functional Communication
Reading, England, United Kingdom · On-site
Clinical Supply Logistics Specialist - Full time office based role in Harlow, Essex ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to…
Skills: Clinical Supply Logistics, GMP Compliance, GDP Compliance, GCP Compliance, Inventory Management
Reading, England, United Kingdom · Remote Solely
The mission of Speechify is to make sure that reading is never a barrier to learning. Over 50 million people use Speechify’s text-to-speech products to turn whatever they’re reading – PDFs, books, Google Docs, news artic…
Skills: Python, Bash, Linux, Docker, Terraform
Reading, England, United Kingdom · Hybrid
Job title: Mechanical Engineer – Wearable Systems & Certification Location: Reading, UK (Hybrid) ABOUT XYZ REALITY ────────────────────────────── XYZ Reality are the creators of the world's first and only engineering-gra…
Skills: SolidWorks, 3D Modelling, ANSI Type II Certification, EN397 Certification, Wearable Product Design
Reading, England, United Kingdom · Remote Solely
In Vivo Toxicologist - UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integri…
Skills: In Vivo Toxicology, Study Monitoring, Project Management, GLP Study Direction, Safety Assessment
Burghfield, England, United Kingdom · On-site
Skills: Dimensional Inspection, Metrology, Engineering
Reading, England, United Kingdom · Hybrid
Project Assistant, IDEA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity…
Skills: Project Coordination, Administrative Support, Meeting Scheduling, Documentation Management, Cross-functional Communication
Burghfield, England, United Kingdom · On-site
$31k–$59k/yr
If you’d like to be considered for this opportunity we encourage you to apply promptly to avoid disappointment as if applications are high the role will close before the closing date given. Metrology Engineer - Dimension…
Skills: Dimensional Inspection, CMM Programming, Quindos, PC-DMIS, GD&T
Reading, England, United Kingdom · On-site
Regulatory Science and Policy Associate - VIE Contract Location: United Kingdom, ReadingTarget start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Li…
Skills: Regulatory Analysis, Policy Monitoring, Advocacy Material Development, Stakeholder Engagement, Cross-functional Collaboration
London, England, United Kingdom · Hybrid
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England. Why IQVIA? Career …
Skills: Site Monitoring, GCP, ICH Guidelines, Subject Recruitment, Protocol Training
Reading, England, United Kingdom · Remote OK
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to h…
Skills: Clinical Support, Medical Device Training, Cardiac Anatomy, Surgical Troubleshooting, Case Coverage
Reading, England, United Kingdom · Remote OK
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to h…
Skills: Medical Device Sales, Cardiac Clinical Expertise, KOL Development, Clinical Selling, Strategic Planning
Reading, England, United Kingdom · Hybrid
Kenvue is currently recruiting for a: Regulatory Affairs Specialist What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of…
Skills: Regulatory Strategy, Drug Application Submission, MRP, DCP, Workshare
Reading, England, United Kingdom · Hybrid
Job Title: Senior Regulatory Affairs Officer Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional & Non-Promotional Materials R…
Skills: Promotional Material Review, Non-Promotional Material Review, ABPI Code of Practice, IPHA Code of Practice, 4M-PromoMats
Sofia, Sofia-City, Bulgaria · Hybrid
Senior Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity,…
Skills: Project Management, Programme Management, Stakeholder Collaboration, Cross-functional Team Leadership, Mentoring
Reading, England, United Kingdom · Hybrid
At OQC, we aren’t just theorising about the future; we’re building it. Born from a philosophy of bold innovation, we’ve successfully transitioned quantum computing from an academic dream into a commercial reality. The mo…
Skills: Project Engineering, Facility Layout Planning, Equipment Procurement, CAD, Contractor Management
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The Clinical Trials Assistant supports Local Trial Managers and CRAs by tracking trial progress and managing study data, budgets, and investigational products. Key duties include maintaining the Trial Master File and managing clinical data flow and project communications.
Candidates must have a degree in life sciences or equivalent experience and previous CTA experience. Proficiency in GCP, ICH guidelines, and Microsoft Office is required, along with strong English communication skills.
The Clinical Trials Assistant will play a vital role in supporting Local Trial Managers and Clinical Research Associates.
Key deliverables include tracking progress of the clinical trial, managing study data, budget, investigational products, mailings and correspondence and other relevant tasks in support of the Local Trial Managers and Clinical Research Associates.
Candidates must be able to commute to sponsor site for on site work in Buckinghamshire for hybrid working. We are seeking candidates with previous CTA experience to hit the ground running.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
There are currently 53 open science & research positions in Reading, United Kingdom listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include ICON plc, IQVIA, Oxford Quantum Circuits (OQC), Sanofi, AWE, among others. Browse the listings above to see every active employer.
Yes — 39 of the 53 open science & research positions offer remote or hybrid work (13 remote, 26 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
