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 Site Contracts Manager (Contract Analyst) you will be responsible for preparing, negotiating and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts

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 member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Please note we are looking for candidates who has 1-1.5 years minimum of indepdant monitoring experience. Ideally with focus on phase 1 studies.

Title: Clinical Biospecimen Scientist  Location: UK, Bulgaria, Spain and Poland - homebased  Fully sponsor dedicated    As a Biospecimen Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare...

Study Start Up Associate I - Home Based- South Korea   As a (SSUA I) 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...

Site Activation Partner Location: Taiwan, flexible WFH 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 our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too. Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

Role: Clinical Trial Associate  Location:Sydney, hybrid   As a Clinical Trial Associate you will have the opportunity to work with one of the world’s leading pharma & biotech companies, helping them advance new drugs and devices.  

Senior Regulatory Affairs Specialist (CMC author) - Homebased in UK, Poland, Spain or Germany    As a Senior Regulatory Affairs Specialist (CMC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   We are seeking a highly motivated and qualified regulatory CMC author/writer for the Global

As a Site Activation Partner you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Le partenaire d'activation du centre de l’étude est chargé de soutenir les activités opérationnelles liées à l’évaluation, l'activation, l'initiation, la surveillance et la clôture des centres/études des chercheurs assignés, afin de garantir le respect des délais de l’étude et conformément aux lois, aux bonnes pratiques cliniques et aux normes en...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

We are currently seeking a Site Engagement Liaison to join our diverse and dynamic team. As a Site Engagement Liaison at ICON, you will play a pivotal role in fostering relationships with clinical trial sites, enhancing site engagement, and contributing to the advancement of inNvative treatments and therapies.

We are currently seeking a Site Engagement Liaison to join our diverse and dynamic team. As a Site Engagement Liaison at ICON, you will play a pivotal role in fostering relationships with clinical trial sites, enhancing site engagement, and contributing to the advancement of inNvative treatments and therapies.

We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of inNvative treatments and therapies.

As a Site Activation Partner/ Study Start Up Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. 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 our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too. Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our...

As a Site Engagement Liaison 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.

We have a new and exciting opportunity for a Senior Global Clinical Project Manager to join a FSP program sponsor dedicated to a Global Pharma.  This is a permanent role through ICON and home-based.    You must already be working within a Pharma or CRO setting with at least 10 years of Global Project Management expertise.   Countries considered: France, Germany, Italy, Spain, Poland, UK, Bulgaria

At ICON we currently have an exciting opportunity on a sponsor dedicated Pharma client who is looking for a Senior Global Clinical Trial Lead to join their growing team. This is a permanent role through ICON and home-based.    MUST come from a clinical research background with at least 7 years experience working within a Pharma or CRO working 4 years as a global CTM/ Project Manager.   Countries we will only consider: France, Germany, Italy, Netherlands, Poland, UK, Bulgaria

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 Risk Based Quality Management Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.