ICON’s FSP group is recruiting a handful of additional UK-based Global Trial Managers to augment their existing GTM team and manage a diverse range of client protocols. You will be partnered with an innovative global biotechnology company focused on areas of unmet medical need, with the ambition to reduce the social and economic burden of disease in today’s society. -

*Luton - office-based position available*   Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Senior Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and a solid understanding of clinical research.   You will be partnering...

  Study Start-up Associate ensures that patients will have access to our clinical trials with the aim of making life better for our patients. The Associate is accountable for obtaining all approvals (Competent Authority and Ethical Review Board) to run the trial in the EMEA and AMERIT Regions. The Associate will also have responsibility to ensure the investigator sites meet the requirement to enroll the study participants in the clinical trial and support maintenance and closeout activities. The Associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File. Additional local responsibilities may be required as...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Clinical Trial Assistant assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Site Contracts Manager (Contract Analyst) you will be responsible for preparing, negotiating and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts

We have a new and exciting opportunity for a Senior Global Clinical Project Manager to join a FSP program sponsor dedicated to a Global Pharma.  This is a permanent role through ICON and home-based.    You must already be working within a Pharma or CRO setting with at least 10 years of Global Project Management expertise.   Countries considered: France, Germany, Italy, Spain, Poland, UK, Bulgaria

At ICON we currently have an exciting opportunity on a sponsor dedicated Pharma client who is looking for a Senior Global Clinical Trial Lead to join their growing team. This is a permanent role through ICON and home-based.    MUST come from a clinical research background with at least 7 years experience working within a Pharma or CRO working 4 years as a global CTM/ Project Manager.   Countries we will only consider: France, Germany, Italy, Netherlands, Poland, UK, Bulgaria

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to bring life-changing treatments to patients faster.   This is your opportunity to be part of an exclusive, high-impact program where you can lead by example and shape the standard for clinical excellence.   -

As a Clinical Trial Assistant you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.   We are currently looking for a Clinical Trial...

As a Clinical Data Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Rave Database Developer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. 

UK-Based In Vitro Diagnostics (Senior level) CRA required to compliment the existing team of IVD CRAs. Target candidate profiles are >BSc educated UK-based experienced CRAs (with a Lab-based background).   You will be partnering with one client focused on developing innovative medicines and diagnostics in areas such as oncology, cardiovascular, ophthalmology, immunology, CNS and infectious...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We're hiring a Contract Analyst I for a client-dedicated, home-based role in France.

As a Clinical Research Coordinator (SMAII) located in the area Eindhoven you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are hiring a Clinical Research Lead, sponsor dedicated in the area Utrecht  

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager within the Early Hematology team to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the project delivery of clinical studies.   The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are hiring a Clinical Trial Manager, sponsor dedicated (Eindhoven area)Position Summary: The Clinical Trial  Manager plays a key role in ensuring high-quality clinical study execution across all active clinical research initiatives. You will lead, support, and manage clinical studies to generate critical clinical evidence, aligned with business goals and regulatory compliance requirements. The role requires close collaboration with cross-functional teams, effective use of...