Role: CRA II Location: Sydney/ Australia (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 Study Delivery Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Role’s alignment with equivalent positions in the pharma industry (in both locations) and internally with ClinOps , in regard to scope and experience Role’s positioning in the Study Delivery Team structure and against their key stakeholders, also in relation to the Study Delivery Specialist and Study Delivery Associate Expectation for the role to have a broader influence on the business, by contributing to continuous improvement initiatives across processes and systems

As Site Management Associate I (SMA I), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    You will be dedicated resource to one of our clients, be embedded in their working environment, systems and processes. You will be engaged in a wide range of interesting and challenging tasks.  

As Site Management Associate I (SMA I), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    You will be dedicated resource to one of our clients, be embedded in their working environment, systems and processes. You will be engaged in a wide range of interesting and challenging tasks.  

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 Senior Feasibility Specialist 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 Research Associate (CRA) in Paris/Ile-de-France!

Join ICON plc as a Clinical Research Associate (CRA) in Paris/Ile-de-France!

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 CRA 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.   

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.

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

Jr Statistical Programmer Location: Bangalore-Homebased   As a Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Senior Statistical Programmer Location: Bangalore-Homebased   As a Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Statistical Programmer 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 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.  

Senior Statistical Programmer  Location: Bangalore/Chennai/Trivandrum-Hybrid   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...

As a Clinical Operations Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.The Clinical Operations Manager is critical as the main provider of CRA oversight as well as CRA career development and progression.  As a People Leader, COMs ensure high performance, adherence to performance metrics and quality of monitoring while supporting career development.

Experienced, UK-based CRA/clinical research associate required to augment existing Oncology CRA team, for pharmaceutical and biotechnology company company partner.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.