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.  

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.   En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.

As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.   En tant qu’ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.

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 Clinical Research Associate.    ICON plc est une organisation de premier plan spécialisée en intelligence en santé et en recherche clinique. Nous sommes fiers de favoriser un environnement inclusif qui stimule l’innovation et...

As a Site Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.   En tant que gestionnaire de site, vous vous joindrez à la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en soins de santé.

As a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and...

As a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and...

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

As a Clinical Research Associate (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.  

As a Local Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true “one team” approach that provides limitless opportunity to develop through training, mentorship, and support from...

As a Clinical Trial Manager, you will be leading the Local Study Team(s) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Procedural Documents and international guidelines such as ICH-GCP as well as relevant local regulations. In addition to leading Local study teams, the CTM may perform site monitoring as needed to support the flexible capacity model.

As a Principal Medical Writer  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   This is a single sponsor dedicated opportunity to one of top-5 pharma companies and is home based.

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.   Job Title: Manager, Clinical Systems Location : Bangalore

As a Clinical Trial Assistant 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 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...

We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting the safety monitoring and reporting of pharmaceutical products. You will contribute to ensuring the safety and efficacy of therapies by assisting in the collection, analysis, and communication of safety data in compliance with regulatory requirements.  

We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting the safety monitoring and reporting of pharmaceutical products. You will contribute to ensuring the safety and efficacy of therapies by assisting in the collection, analysis, and communication of safety data in compliance with regulatory requirements.

As a 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 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.   Youwill be joiningoneofour