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.
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
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
As a Clinical System Lead you would lead and direct one or more project teams in the planning, development, implementation and go-live of clinical system solutions for our biotech and pha
Full Job Description
Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move
As Principal Biostatistician, you will execute diverse statistical tasks supporting the clinical development programs. You will be involved throughout the full clinical trial process, from study de
As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standar
CRA II or Senior CRA
Officebased- Johannesberg/Durban or Homebased
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance
All our team members have the independence to get the job done with support from the experienced leadership team when you need it. If you want a career with a difference, ICON Strategic Solutions is t
Job Overview
The Senior Clinical System Designer uses technical, industrial, and interpersonal skills to create case report forms (CRFs) for trials.
Lead and serve as main point of contact re
The Role:
The Principal Statistical Programmer will be aligned to a project leadership or technical expertise role, encompassing the following responsibilities
The Principal Statistical Progr
