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

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

Site Care Partner 1 Location: Mumbai (office-based)   As a Site Care Partner, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with one of the world’s premier...

The Study Startup Associate is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards. Responsibility within a country and may span over more than 1 country depending on the geographical region and business needs.

As a Medicl Science Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with a global pharmaceutical company committed to using innovative science to help those with serious and rare diseases. This team prides itself on a family oriented and cohesive environment. If feeling valued and knowing that your voice matters is important to you, this program may be an excellent option....

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 CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with a client focused on developing innovative medicines and diagnostics in areas such as oncology, cardiovascular, ophthalmology, immunology, CNS and infectious diseases.

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.

Title: Principal Clinical Research Associate  Location: United Kingdom, remote Sponsor dedicated    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...

Clinical Trial Study Support Specialist (0.5 FTE) Location: Brisbane or Melbourne (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), permanent employment. 

As a Regultory Affairs Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with a global pharmaceutical client that creates value through innovation with a clear goal: to provide more health and improve the lives of both humans and animals.

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

As a Randomization & Trial Supply Manager (RTSM) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The LTM is the primary point of contact at a country level for assigned studies. The LTM isresponsible for coordinating and leading the local trial team in order to deliver quality data and trial documents/records that are compliant with assigned protocol, codes of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs) and regulatory requirements. LTM actively contributes to process improvement; training and...

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

The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives

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.

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.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio inmultiple therapeutic areas. 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...

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