Current jobs related to Clinical Trial Project Manager - Reading Berkshire - ICON
-
Clinical Trials Supply Chain Manager
2 weeks ago
Reading, Reading, United Kingdom IQVIA Full timeJob OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department and processes.Key ResponsibilitiesInterpret clinical trial...
-
Clinical Trials Supply Chain Manager
2 weeks ago
Reading, Reading, United Kingdom IQVIA Full timeJob OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department and processes.Key ResponsibilitiesInterpret clinical trial...
-
Senior Clinical Trial Assistant
4 months ago
Reading, United Kingdom Novasyte Full timeDo you want to grow your career with the World’s largest CRO? Our Sponsor Dedicated team are recruiting for a Senior Clinical Trial Assistant to join us on our mission to drive healthcare forward. IQVIA offer genuine career progression (named on LinkedIn’s Top Companies: The 25 best workplaces to grow your career in the UK), supportive leadership, team...
-
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob SummaryWe are seeking a highly skilled Regulatory Manager to join our team at IQVIA Argentina. As a key member of our Clinical Trials Regulatory Management team, you will be responsible for preparing and reviewing regulatory documents to support clinical trial submissions.Key ResponsibilitiesAct as a Clinical Trial Regulatory Manager (CTRM) on complex...
-
Reading, Reading, United Kingdom IQVIA Argentina Full timeJob SummaryWe are seeking a highly skilled Regulatory Manager to join our team at IQVIA Argentina. As a key member of our Clinical Trials Regulatory Management team, you will be responsible for preparing and reviewing regulatory documents to support clinical trial submissions.Key ResponsibilitiesAct as a Clinical Trial Regulatory Manager (CTRM) on complex...
-
Clinical Trial Coordinator
5 days ago
Reading, United Kingdom Pharmiweb Full timeOur sponsor dedicated (cFSP) team are seeking a Clinical Trial Coordinator to join us on our mission to drive healthcare forward.Hybrid working on offer, with 3 days per week required on-site in Central London with the sponsor, a large multinational pharmaceutical.The Clinical Trial Coordinator will perform a variety of clinical procedures to collect,...
-
Clinical Trial Regulatory Lead
3 weeks ago
Slough, Berkshire, United Kingdom EPM Scientific Full timeABOUT THE COMPANY We are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development. Located...
-
Clinical Trial Regulatory Lead
3 weeks ago
Slough, Berkshire, United Kingdom EPM Scientific Full timeABOUT THE COMPANY We are a pioneering pharmaceutical company dedicated to the discovery, development, and delivery of innovative treatments for patients with rare and life-threatening diseases. Our mission is to transform the lives of those affected by these challenging conditions through cutting-edge research and patient-centric drug development. Located...
-
Clinical Trial Vendor Manager
5 days ago
Reading, Reading, United Kingdom IQVIA Full timeAbout the RoleWe are seeking a highly skilled Clinical Trial Vendor Manager to join our team at IQVIA. As a key member of our clinical operations team, you will play a critical role in ensuring the success of our clinical trials by managing vendor relationships and ensuring compliance with regulatory requirements.Key Responsibilities:Vendor Management:...
-
Clinical Trial Vendor Manager
5 days ago
Reading, Reading, United Kingdom IQVIA Full timeAbout the RoleWe are seeking a highly skilled Clinical Trial Vendor Manager to join our team at IQVIA. As a key member of our clinical operations team, you will play a critical role in ensuring the success of our clinical trials by managing vendor relationships and ensuring compliance with regulatory requirements.Key Responsibilities:Vendor Management:...
-
Global Clinical Trial Lead
7 days ago
Reading, Reading, United Kingdom IQVIA Full timeJob PurposeThe Global Clinical Trial Lead is the leader of the cross-functional clinical trial team, guiding planning and management of assigned clinical studies end-to-end to achieve objectives. Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the clinical trial team. Oversees...
-
Global Clinical Trial Lead
7 days ago
Reading, Reading, United Kingdom IQVIA Full timeJob PurposeThe Global Clinical Trial Lead is the leader of the cross-functional clinical trial team, guiding planning and management of assigned clinical studies end-to-end to achieve objectives. Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the clinical trial team. Oversees...
-
Clinical Trials Data Administrator
3 weeks ago
Bracknell, Berkshire, United Kingdom Boehringer Ingelheim Full timeClinical Trial Data Administrator - 12 month Contact The Clinical Trial Data Administrator leads Quality Medicine (QM) data, risk and project management activities. In this context, the role will: -Leads the preparation, execution and post-processing of medium complexity projects and contributes to strategic initiatives within global QM. -Leads...
-
Clinical Trials Data Administrator
4 weeks ago
Bracknell, Berkshire, United Kingdom Boehringer Ingelheim Full timeClinical Trial Data Administrator - 12 month Contact The Clinical Trial Data Administrator leads Quality Medicine (QM) data, risk and project management activities. In this context, the role will: -Leads the preparation, execution and post-processing of medium complexity projects and contributes to strategic initiatives within global QM. -Leads...
-
Clinical Trial Coordinator
3 months ago
Reading, United Kingdom Clintec Full timeJob Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. This role offers hybrid working, with 2-3 days on site...
-
Global Clinical Trial Lead
3 weeks ago
Reading, Reading, United Kingdom IQVIA Full timeJob PurposeThe Global Clinical Trial Lead is responsible for overseeing the planning and management of clinical studies from start to finish. This involves guiding cross-functional teams and ensuring the successful execution of studies to meet business objectives.Key ResponsibilitiesDevelop and implement clinical trial strategies to achieve business...
-
Medical Devices Regulatory Project Manager
4 weeks ago
Reading, Berkshire, United Kingdom Pharma Partners Recruitment Ltd Full timeRegulatory Affairs Project Manager – UK/IE A Top 10 Pharmaceutical business in Berkshire are seeking a Regulatory Affairs Project Manager. This is a UK/IE affiliate role and will work across an Oncology portfolio. Lifecycle management of applicable products and management of Clinical Trial activities with the MHRA. Reviews promotional,...
-
Clinical Supply Chain Manager
11 hours ago
Reading, Reading, United Kingdom IQVIA Full timeJob OverviewThe Clinical Supply Chain Manager plays a pivotal role in ensuring the seamless execution of clinical trial supply chain projects. This position requires a strategic thinker who can interpret clinical trial protocols to create effective supply chain solutions.Key ResponsibilitiesDevelop and execute clinical trial supply chain strategies to meet...
-
Clinical Supply Chain Manager
9 hours ago
Reading, Reading, United Kingdom IQVIA Full timeJob OverviewThe Clinical Supply Chain Manager plays a pivotal role in ensuring the seamless execution of clinical trial supply chain projects. This position requires a strategic thinker who can interpret clinical trial protocols to create effective supply chain solutions.Key ResponsibilitiesDevelop and execute clinical trial supply chain strategies to meet...
-
Clinical Project Associate
5 months ago
Reading, United Kingdom ICON Full timeAs a Clinical Project Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The CPA will interact on a global scale within the study team and clinical team. The CPA sphere of influence and communication will include the Global Clinical Lead, the Clinical Project Manager,...
Clinical Trial Project Manager
4 months ago
Clinical Trial Manager position, UK based – In Vitro Diagnostics/Medical Devices
You will be partnering with a well-known leader in in vitro diagnostics, who offer a broad range of innovative ways for hospitals, labs, blood banks and clinics to diagnose and monitor health conditions with greater accuracy, speed, convenience and cost-efficiency. The result is smarter decisions for physicians and better health outcomes for patients.
Here in the ICON Strategic Solutions team, we are in an established partnership to supply a permanent, full-time, UK-based Clinical Trial Manager with considerable Medical Devices experience.
Designs, plans and executes study management and clinical monitoring activities of large-scale trials in support of IVDR submissions for diagnostic devices.
Prepare and author IVDR gap assessments and Clinical Performance Reports.
Provide comprehensive support of all operational aspects of clinical trials for which he/she is responsible for, including the review and approval of protocols and study-related documents (e.g., Regulatory Binder, Work Instructions, CRF Completion Guidelines, etc.)
Effectively lead the operational clinical team for assigned studies and delegate appropriate tasks, assignments, and responsibilities to subordinates.
Develop and administer budgets, schedules and performance requirements for assigned studies.
Manage Clinical Research Organization (CRO) interactions, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data management) as applicable.
Collaborate with the Legal Department to develop study contract templates across the trial and specifically for each study site.
Develops the Site Monitoring Plan and ensures CRA compliance with the plan
Reviews monitoring visit reports and assures adherence to study timelines for report submission and finalization
Participates in site start-up activities including site selection and regulatory document collection, review, approval and tracking; Additional project and tasks as determined by department and organizational needs
Travel may be approximately 20-50%
Master’s degree or Medical Technology Certification, familiarity with IVDR, experience with managing external CROs and on-site monitoring experience of IVD clinical studies is preferred.
Strong technical writing skills
Advanced knowledge of clinical trial practices and regulations
Advanced knowledge of clinical trial, design, clinical trial databases, and data analysis for IVD clinical trials
Proficient computer skills including Microsoft Office Suite
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
LI-Remote
#
