As a Clinical 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.

As a CRA  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. • Identify, select, initiate and closeout appropriate investigational sites for clinical studies. • Monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with ICON SOPs/WPs applicable regulations and the principles of ICH-GCP. • Provide a benchmark of monitoring competence to inexperienced/less-experienced colleagues.

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.

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

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

Join ICON plc as a Clinical Trial Manager (CTM) in Paris/Ile-de-France!   ICON plc is a global leader in healthcare intelligence and clinical research. From molecule to medicine, we provide outsourced services to pharmaceutical,...

Join ICON plc as a Clinical Trial Manager (CTM) in Paris/Ile-de-France!   ICON plc is a global leader in healthcare intelligence and clinical research. From molecule to medicine, we provide outsourced services to pharmaceutical,...

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence   You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society...

We are seeking motivated, reliable, and dedicated Clinical Research Associates (CRAs) with at least 1 year of experience as a CRA within a CRO. Ideally, you should have experience in Oncology and Onco-Hematology, although...

We are seeking motivated, reliable, and dedicated Clinical Research Associates (CRAs) with at least 1 year of experience as a CRA within a CRO. Ideally, you should have experience in Oncology and Onco-Hematology, although...

Regional CTA submission manager (EU CTR) - Homebased in UK or Europe An exciting new role with ICON within Our regulatory team working on high profile Pharma projects with a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market.   The Regional CTA Submission Manager (CTA-SM) is accountable for working with contributing to business lines to lead...

Clinical Trial Assistant Location: Sydney (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 government and public health organisations.

As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team...

Regulatory affairs CTA submission manager -  (Global) - Homebased in EMEA An exciting new role with ICON within Our regulatory team working on high profile Pharma projects with a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market.   The Global CTA Submission Manager (CTA-SM) is accountable for working with contributing to...

As a Clinical Research Associate (CRA) will have local responsibility for the delivery of the studies at allocated sites and be an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Leader to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.

Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move from one job to another and the process involves careful consideration. At ICON, we care about our people as they are the key to our success and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term career. All our team members have the independence to get the job done with support from the experienced leadership team when you...

Scotland or Northern UK-Based In Vitro Diagnostics CRA required to augment existing team of IVD CRAs. Target candidate profiles are >BSc educated UK-based experienced CRAs to monitor at sites in Scotland only.   You will be partnering with a client focused on developing innovative medicines and diagnostics in areas such as oncology, cardiovascular, ophthalmology, immunology, CNS and...