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.
The Role:
Lead KOM with internal teams for Site Audit finding review.
Ensure that audit results are formally recorded and reported and that corrective/preventive actions are documented.
OVERVIEW OF THE ROLE:
The Senior Clinical Data Science Lead (Senior CDSL) serves as the primary contact for internal and external team members regarding clinical data science data review activit
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 &
Site Activation Lead
As a Site Activation Lead at ICON, you would advance clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for
Responsibilities:
Recognize, exemplify and adhere to ICON's values which center on Integrity, Accountability & Delivery, Collaboration, Partnership and Own IT@ICON
Manage Projects, Peo
The role:
Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
Submitting protocol, consent documents for ethics/IRB approval, as well as prep
The role
You will lead/project manage multi-disciplinary teams on assigned projects.
Be responsible for developing, maintaining and validating standard data structure and software.
Design an
The Role:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new phar
Responsibilities:
Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance wit
The role:
The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study within Italy .
The CTM oversees the clinical portion of the budget, develops monitorin
Responsibilities:
Planning, managing and execution of statistical programming deliverables in clinical trial and non-trial activities in the project
Providing input to authority required docum
Responsibilities
Lead the planning and implementation of cross-functional eCOA project(s).
Facilitate the definition of eCOA project scope, goals and deliverables.
Define project tasks and r
The Role:
Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
Submissi
About the role
As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will
About the role
As a Clinical Quality and Training Manager Sub-Saharan Africa region(South Africa Based), you will be joining the world’s largest & most comprehensive clinical research org
About the role
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharm
Role:
Recognize, exemplify and adhere to ICON's values, which center on our commitment to People, Clients and Performance
Ability to work on study teams that are often virtual, multi-cultur
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
