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

As a Clinical Trial Assitant,  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 Clinical Research Associate, you will be partnering with a biotech company that is at the epicentre of innovative drug development.

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

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.

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

We are currently seeking a Study Start Up Specialist to join our diverse and dynamic team. As a Study Start Up Specialist, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will play a...

As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: Taipei, client office, Flexible WFH

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

**Role is open for HOMEBASED setup**   ICON PLC is seeking a highly skilled and experienced Principal Clinical Data Science Programmer to join our team in Manila. The ideal candidate will have over 4 years of experience working within Data Warehouse platforms in a regulated industry, specifically within a clinical trial environment (IDAR). This role demands a deep understanding of data visualization tools, scripting languages, and SDTM data structures, along with the ability to work independently on complex assignments.

ICON PLC is seeking a highly skilled and experienced Senior Lead Clinical Data Science Programmer to join our team. The ideal candidate will have over 4 years of experience working within Data Warehouse platforms in a regulated industry, specifically within a clinical trial environment (IDAR). This role demands a deep understanding of data visualization tools, scripting languages, and SDTM data structures, along with the ability to work independently on complex assignments.

As a Clinical Scientist,  you will provide scientific, clinical, and operational input to early and late-stage clinical development programs with an emphasis on protocol-specific, in-life clinical data monitoring activities. This role will work on cross-functional study teams on design, execution, and monitoring of clinical trials, as well as data interpretation and communication. This role will also serve as a point of contact for investigators in day-to-day clinical study needs.

As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Exciting opportunity to join our expanding team of Regional Clinical Scientists.  Our sponsor is paving the way with ground-breaking novel treatments in Cystic Fibrosis and expanding research into other rare diseases where we plan to make a difference in more patients lives.   

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving...

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    A CRA 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...

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.

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

As a Senior CDC you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  We are looking for Immediate Joiners in Chennai & Bangalore (Hybrid).

We are constantly looking for motivated, reliable and dedicated CTAs who can demonstrate a first experience as a Clinical Trial Assistant within the pharmaceutical industry or a CRO.   As a Clinical Trial Assistant you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common...

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