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

(Sr.) Regulatory Affairs Specialist, Seoul, South Korea   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 lives.

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

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 Lead TMF Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The role independently maintains the Trial Master Files for assigned studies, participating in end-to-end TMF management activities, including adherence to organizational TMF standards and study-level quality control reviews, and facilitating issue resolution.    

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

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

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

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

As a sponsor dedicated Clinical Research Associate 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 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.

Statistical Programming Team Lead Location: Bangalore/Chennai/Trivandrum-Hybrid   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...

Clinical Trial Study Support Specialist (0.5 FTE) Location: Blacktown (Sydney, Australia); on-site   As Study Site Support Specialist, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence in a part-time (0.5 FTE), fixed-term employment (6 months, likely to be extended). 

As a Senior Biostatistician 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.

Home-Based, Seoul, South Korea   As a (Senior CRA) 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 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

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.

Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team, for pharmaceutical and biotechnology company company partner.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

As a Site Management Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will provide support to the clinical trial team at the global level impacting directly project's success