Job title: Associate Project Manager Working location: Taipei, Taiwan, Client office based   Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with...

Contract Analyst - Clinical Trials Location: Australia (home-based)   As an experienced Contracts Specialist, 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.   You will...

Contract Analyst II (Contract & Budget Nego) - Home Based - South Korea   As a (Contract Analyst II) 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and...

Clinical Research Associate (Oncology Team) 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 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

ICON’s FSP group is recruiting a handful of additional UK-based Global Trial Managers to augment their existing GTM team and manage a diverse range of client protocols. You will be partnered with an innovative global biotechnology company focused on areas of unmet medical need, with the ambition to reduce the social and economic burden of disease in today’s society. -

As a Senior CRA / Clinical Site Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You’ll utilise your extensive therapeutic knowledge in Oncology to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.

As a Senior Clinical Validation Analyst 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

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.

Title: CRAII  Location: Sydney, Melbourne or Brisbane (home-based) preferred.    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 Clinical Validation Analyst 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

As a Clinical Validation Analyst 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

As a Senior Clinical Validation Analyst 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 worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally.

As a Global CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: ICON office, fully office based. **No flexible to work from home.

As a Global CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: ICON office, fully office based. **No flexible to work from home.

As a Assoicate Director of Vendor Management you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Job title:Study Start Up Manager  Location: UK (fully homebased) Fully sponsor dedicated   As a Study Start Up Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

This Senior Statistician position will provide statistical support for projects in the Vaccines Therapeutic Area. The qualified candidate will collaborate and work closely with project / study teams and provide statistical expertise in designing research concepts, developing protocols, writing statistical analysis plans, performing statistical analyses, interpreting and presenting results, writing/reviewing reports, and publishing manuscripts through co-authorship.  The candidate may also provide support in regulatory submissions including responses to regulatory queries.  A successful candidate will make contributions through quantitative and creative thinking as...

This Senior Statistician position will provide statistical support for projects in the Vaccines Therapeutic Area. The qualified candidate will collaborate and work closely with project / study teams and provide statistical expertise in designing research concepts, developing protocols, writing statistical analysis plans, performing statistical analyses, interpreting and presenting results, writing/reviewing reports, and publishing manuscripts through co-authorship.  The candidate may also provide support in regulatory submissions including responses to regulatory queries.  A successful candidate will make contributions through quantitative and creative thinking as...

We are currently seeking a CTA to join our diverse and dynamic team. As a CTA 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 inNvative treatments and therapies.