As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration, and performance.  

As a Drug Safety Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be joining one of the global healthcare leaders that has been discovering and developing medicines and treatments for well over a century. You will be part of a global team that is committed to make life better for people around the world. We share a vision of bringing treatment and medicine to millions alongside develop healthcare knowledge and improve live.   As a Drug Safety Associate at ICON, you’ll work within a large-scale, fast-paced environment as part of our newly created case processing hub in Makati. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. This role will offer a hyrbid work from home and office arrangement.

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.   The Statistical Programmer II will provide programming leadership for high complexity studies including effective resource planning, work allocation and progress tracking to ensure project timelines and quality targets are consistently achieved.   In this client facing role, the Statistical Programmer II will be responsible for writing programming specifications and the development/QC of statistical programs and applying extensive domain and therapeutic knowledge in the programming of datasets, tables, figures and listings to ensure quality and accuracy.

At ICON Strategic Solutions, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Clinical Research Associate Guangzhou office based

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Clinical Research Associate Chengdu office based

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Clinical Research Associate Beijing office based

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Clinical Research Associate Shanghai office based

Position Summary:   Title: Senior Project Associate Location: Chennai worktype: Officebased - Responsible to ensure timely support and solution to Operations Managers and/or ICON stakeholders globally with FSE administration. - Responsible to achieve SLA’s set in terms of meeting the standard quality, timelines and efficiency with day to day Operations Support activities. - Lead and drive process improvement initiatives on end to end business support activities and drive operational efficiencies using data analytics, problem solving and basic automation skills using MS Excel and VBA Macros

As a Senior Clinical Trial 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.   You will join one of the fastest growing biotech working on innovative early phase clinical trials.

For a fully sponsor-embedded opportunity, ICON are looking for Clinical Research Associate to join our Team. In this role, You will be working alongside a world-leading pharmaceutical company. This 19- year partnership is focused on leveraging cutting-edge science to make a positive impact in the therapeutic areas of cancer, cardio-metabolic, vaccines, and oncology, which makes up 70% of their portfolio. If you’re looking to make difference, this could be the career destination for you.   At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Title – Senior Clinical Trial Assistant Location - Johannesburg South Africa Sponsor dedicated   ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organization's. With our patients at the center 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. This role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools. The role is critical to meet planned Site Ready dates, including assisting with the preparation of submission packages to IRB/ERC and Health Authorities. The role will collaborate at local level closely with COM, CRM and CRA. The person acts as process Subject Matter Expert (SME), making recommendations for continuous improvement, providing training as appropriate/required and mentoring junior CTCs.    

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.

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 Engagement Liaison (SEL) will be responsible for developing relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials. 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 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.   Youwill be joiningoneofourclients, a biotechnologycompanythatis at theepicenterof innovative drugdevelopment. This program is for you if you are looking for an innovative environment where you can develop and grow while making a valued contribution to improving people´s lives.   You will be joining as the country Project Manager and will be responbile for the operational delivery of strategic clinical studies assigned to Germany, to support the client's pipeline, in accordance with ICH/GCP, SOPs, local operating guidelines and local requirements, as applicable.   #LI-SC3

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 Clinical Research Associate 2 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.

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 Clinical Research Associate II at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.   You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

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.

Duties will be variable depending on the nature of the projects to be undertaken. These will mainly fall within the areas of Pharmaceutical, Biotechnology or Biologics Regulatory Affairs but may be in other related areas. • As member of the Regulatory Submissions team, you will contribute to at least one of the following activities: • Preparation, compilation and submission of CT /IND, MAA I NOA. Variations/ lifecycle submissions, DSUR, PSUR, renewals, agency briefing documentation • Management and Implementation of label review, translation requirements, fee requirements etc. for regulatory submissions • Input to the Reg Intel function • Readability testing • IMPD / IB Core Doc review, labelling review for CT • May work either as part of Regulatory Submissions team or as part of a regulatory or cross-functional team depending on the size and nature of project • May support business development activities