Study Start Up Associate II Location: Australia (home-based)   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.  

The RBSM Central Risk  plays a critical role contributing to the embedding, growth and continuous improvement of the clinical study risk management process. The RBSM Central Risk r is responsible for supporting the study teams with initial risk assessment process, ongoing assessment of Key Risk Indicators (KRIs) to identify issues and emerging risks in clinical trial variables (trends / outliers / poor performing sites) through the review of aggregate data, and leading the monthly study risk review process. The RBSM demonstrates a strong degree of technical and clinical trial expertise while...

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.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work in a solid partnership and an environment driven...

Site Engagement Liaison Location: Sydney/ Melbourne (home-based)   As a Site Engagement Liaison, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with one of the...

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

We are constantly looking for motivated, reliable and dedicated CRAs who can demonstrate at least 12 months independent external monitoring of commercial studies (or a mix of commercial clinical studies) ideally in Oncology and Hematology. Other therapeutic areas are also of interest, especially if gained on phase I - II or III commercial trials.   As a Clinical Research Associate

The Study Start-Up Associate (SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements. At the Senior level, the Study Start Up Associate will manage and lead all activities listed above and will ensure that all activities meet Sponsor and PRA expectations and are delivered in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.

The Study Start-Up Associate (SSUA) performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements. At the Senior level, the Study Start Up Associate will manage and lead all activities listed above and will ensure that all activities meet Sponsor and PRA expectations and are delivered in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.

We are constantly looking for motivated, reliable and dedicated CRAs who can demonstrate at least 12 months independent external monitoring of commercial studies (or a mix of commercial clinical studies) ideally in Oncology and Hematology. Other therapeutic areas are also of interest, especially if gained on phase I - II or III commercial trials.   As a Clinical Research Associate

As a Recruitment Strategist 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 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...

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

Home-Based, Seoul, South Korea   As a (CRA II or Senior 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 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.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work in a solid partnership and an environment driven...

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.

Regulatory Affairs Manager, Seoul, South Korea   You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.

This role will focus on ensuring compliance, effective communication, and timely completion of start-up deliverables for clinical trials. Considered candidates will have at least 2 years of experience in clinical trial start-up, strong organizational and communication skills, and the flexibility to take on diverse responsibilities.

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