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:
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
About the role
At ICON Strategic Solutions, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advan
As Senior Biostatistician, you will execute diverse statistical tasks supporting the clinical development programs. The tasks mainly focus on guarantying by means of thorough review outstanding statis
As a Principal Biostatistician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
As a Principal Biostatistician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
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 pharmac
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 pharmac
About the role
As a Site Engagement Liaison(Johannesburg South Africa), you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthca
The Senior Statistical Programmer will provide programming leadership for high complexity studies including effective resource planning, work allocation and progress tracking to ensure project time
We have an incredible opportunity for an experienced Clinical Data Lead to join the team.
The role:
As a member of staff, the employee is encouraged to accept and supply to our culture
