We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives an... read mored improve quality of life.
We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-o
You will be responsible for managing a local clinical team effectively, maximizing resource use to deliver operational, quality, and fiscal targets whilst ensuring employee engagement, retention and g
The Role:
This is a permanent, home-based position available to hire in multiple EMEA countries
The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study.
Overview of the Role:
The Principal Statistical Programmer is responsible for creating, validating, and executing a range of statistical programs and applies extensive domain knowledge in the progr
Overview of the role:
The Principal Biostatistician will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of h
The role:
The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study.
The CTM oversees the clinical portion of the budget, develops monitoring plans &
Role overview:
As a Sr Project Manager you will be expected to contribute towards a culture of business excellence with a focus on quality, scope, timelines adding value to the business and exceedi
Overview of the Role:
The Principal Statistical Programmer will be responsible for creating, validating, and executing a range of statistical programs and applies extensive domain knowled
About the job
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pha
About the job
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharma
Job Functions/Responsibilities
Perform negotiation of legal terms and budget terms for Clinical Study Agreements (“CSA”) (i.e., investigator site agreements)
Perform negotiation of
Study Start Up Clinical Research Associate is responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU CRA is responsible for overseeing
Responsible for leading Local Study Teams within country, in order to effectively deliver on Clinical Studies(Oncology) with regards to budgets, resources, ICH-GCP guidelines and local regulations. Wi
Summary of SDTM Programmers’ responsibilities:
Interact with vendors to receive CRF & external data. Review data transfer specs to ensure data is in a form we can use (SAS compliant va
Key Responsibilities
In line with corporate/regional/Clinical Development Centre (CDC) priorities, plan and conduct clinical quality assurance and clinical training activities to ensure that the
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-o
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you
