As a Sr Study Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

PM To be responsible for the overall direction, coordination, implementation, execution, control and completion of global cross-functional or single service projects ensuring consistency with ICON SOPs, study contracts and budgets

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

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 Senior Feasibility Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

DATA ANALYSIS: • Provide Data Analysis support to Feasibility & Management Teams on all required aspects- Investigator/ Site Feasibility, Patient Recruitment Planning, Monthly Metrics, Specific Projects and Ad-Hoc requests. LEADERSHIP: • Lead Team of Data Analysts being responsible for all tasks executed ensuring highest standards of quality and performance delivery.

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 with a well-known global pharmaceutical company with a strong portfolio in Oncology trials.

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 Research Associate (CRA) - FSP Model, Global Pharma Location: Hong Kong   As a Clinical Research Associate (CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity...

As a Drug Development Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.   You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

The main function of the Junior Project Manager is to improve integrated drug development asset planning by rigorous project plan management within the planning systems across the R&D and Medical enterprise. The Junior Project Manager will provide planning support to the accountable Project Manager working with key epidemiology, data generation, and related functional partners. With support at times from senior colleagues this role will deliver high quality development schedules / plans based on analytical data, benchmarks and information from the Medicine / Vaccine Development & Medical Teams. This position must become a trusted partner to and interact early and closely with the...

As a Clinical Research Associate 2 you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are currently seeking a Senior Patient Safety Specialist to join our diverse and dynamic team. As a Senior Patient Safety Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

This position is responsible for creating and maintaining the Project Plan which contains epidemiology, data generation, and related activity/study timelines, resource and budget forecasts for a specific indication for a medicine or vaccine. The Project Manager will partner with members from Epidemiology, Data Generation, Real World Data & Analytics, Patient Centered Outcomes, Study Delivery and other functions to drive strategic alignment of studies at a project and portfolio level. Collaboration across Research & Development, the Chief Patient Officer Organization, Operations, Finance and others will be a key responsibility of the PM to drive discipline in planning, execution and...

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.

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...

We currently have an exciting new opportunity for an Associate Project Manager to join our growing team, sponsor dedicated. The Associate PM is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management.   This is a permanent role with ICON and fully home-based.  You must be located in the following countries to be consider:  Hungary, Poland, Czech, Spain. 

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.   - Reporting to the Associate Director or Director within FASTR (Feasibility, Activations and Strategy & Tactics of Recruitment), this role will be responsible for providing support to study teams across key programs, to enable acceleration of sponsor clinical studies -

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.