Location: Philippines (Homebased)   Under the direction of the Data Management Lead, the Senior Manager Clinical Data Management is responsible for timely and high-quality data management deliverables supporting the company’s portfolio. They are responsible for conducting oversight of Data Management activities at the project or program level – as performed within the company or by Strategic Partners, CROs or other 3rd Party Vendors - to ensure they meet obligations as described in ICH-GCP and...

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. 

This role is key to the success and consistency of delivery of the clinical phase of the project. Primary point of contact for clinical deliverables for both internal and external customer. Key role to manage clinical operations to highest standard and efficient performance.   Single service project manager for clinical operations. Oversight for day-to-day delivery of of the clinical portion of the project from site identification to database lock e.g. leading the clinical team,...

The Senior contract analyst plays an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical...

Contract & Budget Analyst, Home-based, South Morea   As a (Contract & Budget Analyst) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Global Medical Safety Lead - Homebased in UK or Europe. As a Global Medical Safety Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   ICON is partnering with one of the industry’s...

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

As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies, and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s, and infectious...

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Regulatory Project Manager - Homebased in UK/Europe   As a Regulatory Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   The Regulatory Project Manager collaborates with regional and global cross functional teams to plan, prepare and deliver compliant regulatory submissions, providing support to...

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

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

As a Senior Medical Writer you will be dedicated to one of our global pharmaceutical clients; a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing lifeimproving drugs to market.    We are also reviwing freelance regulatory medical writers based in Ireland.    Please note , this is role is open for Ireland location only.

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

As a Senior Biostatistician I 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.     ICON plc est un chef de file mondial en intelligence en santé et en recherche clinique.

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

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