As a CRA II in Austria 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.

A Senior Medical Writer is a professional who contributes to drug and device development through independently writing, editing, and compiling scientific documents related to clinical trials (narratives and summarize data from biostatical tables/listings). This role may assist with resource management A Senior Medical Writer may reside in either Early Phase or Medical Writing Publishing or MediMedia.  

The Global Clinical Trial Assistant MAO (GCTA MAO) assists with local project management activities of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include assisting with operational aspects of assigned project(s) at the country level for end-to-end project management from start-up through to closeout activities. Further, services will range depending on the therapeutic area and project-specific requirements. Reports to Sponsor Manager or designee, and partners with the Global Trial leader (GTL) to ensure overall study delivery at the country level.

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 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,...

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

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.   We are currently seeking a Clinical Research Associate II Specialist  based in...

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

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.

As a CRA(SSU) 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...

Senior Principal Safety Scientist- Homebased in the UK or Europe   As a Senior Safety Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   ICON is partnering...

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

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

(Sr.) CRA I, II, Home-Based, Seoul, South Korea   As a (Sr. CRAI/II) 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 Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a  CTA in HUNGARY   you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. To be an integral part of the study team by providing administrative and project tracking support to the Project Manager(s) and Clinical Trial Manager(s) with emphasis on supporting inspection readines