We are hiring! Contract and Costings Managers (working on non-Oncology clinical trials), either from home or at our client's Luton office.   It is a very exciting time at ICON – ICON plc is a world-leading healthcare intelligence and clinical research organisation. 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.  

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

As a Graduate Pharmacovigilance Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

As a Manager Pharmacovigilance you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

As a CDC II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Location : Chennai [OFFICE-BASED]  Immediate joiners only

As a Manager, Clinical Trial Transparency 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.

Join ICON plc as a Clinical Trial Manager (CTM) in Paris/Ile-de-France!   ICON plc is a world leader in healthcare intelligence and clinical research. From molecule to medicine, we provide outsourced services to pharmaceutical, biotechnology, medical device, and public health organizations. With a patient-centered focus, we accelerate the development of life-saving drugs and devices that improve quality of life. Our people are our greatest strength and the driving force behind our success. ICON people are passionate about achieving success and ensuring excellence in everything we do. We...

Clinical Research Associate Working Model: Hong Kong Client Office based   As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

As a Clinical Trial Manager at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of treatments and therapies.  

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

Role: CRA II Location: Auckland/ New Zealand (hybrid - working from home and from the sponsor office during onboarding)   As an experienced Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

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-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

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

As a Site Activation Partner 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).

As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will Lead, manage, and coordinate all internal and external writing activities associated with the preparation, compilation, and submission of applications to regulatory authorities globally.

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 ICF Specialist you will be responsible for review, coordination and finalization of Global Informed Consent Form templates for all client clinical studies that are managed by Development Operations. Responsibilities also include supporting CSS Central Services team as needed.

Job title - Central Services Specialist-ICF Location - any of the following: UK, Spain, Poland (fully remote) Fully sponsor dedicated   As a Central Services Specialist-ICF you will be joining the world’s largest & most...

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