As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: Taipei, Taiwan, sponsor office

As a (SDS ) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The revised job description is to reflect: • Role’s alignment with equivalent positions in the pharma industry (in both locations) and internally with ClinOps  in regard to scope and experience • Role’s positioning in the Study Delivery Team structure and against their key stakeholders, also in relation to the Study Delivery Specialist and Study Delivery Associate • Expectation for the role to have a broader influence on the business, by contributing to continuous improvement initiatives across processes and systems

As a Study Delivery Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Role’s alignment with equivalent positions in the pharma industry (in both locations) and internally with ClinOps , in regard to scope and experience Role’s positioning in the Study Delivery Team structure and against their key stakeholders, also in relation to the Study Delivery Specialist and Study Delivery Associate Expectation for the role to have a broader influence on the business, by contributing to continuous improvement initiatives across processes and systems

Prepare, negotiate and finalize agreements and budgets related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

As a Senior Clinical Scientist 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.

Home-based, Location: Mumbai & Delhi    As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will have an opportunity to work in a solid partnership and an environment driven by innovation and...

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...

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

DATA ANALYSIS: • Provide Data Analysis support to Feasibility & Management Teams on all required aspects- Investigator/ Site Feasibility, Patient Recruitment Planning, Monthly Metrics, Specific Projects and Ad-Hoc requests. LEADERSHIP: • Lead Team of Data Analysts being responsible for all tasks executed ensuring highest standards of quality and performance delivery.

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.

We currently have an exciting new opportunity for an Associate Project Manager to join our growing team, sponsor dedicated. The Associate PM is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management.   This is a permanent role with ICON and fully home-based.  You must be located in the following countries to be consider:  Bulgaria, Poland, Spain and...

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    A CRA is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.   You will...

As a Clinical Trial Manager II 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.

As a (Sr.) Clinical Trial Coordinator 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 well.

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 作为临床监查员，您将加入全球最大、最全面的临床研究机构 - ICON 临床监查员  

As Site Management Associate I (SMA I), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    You will be dedicated resource to one of our clients, be embedded in their working environment, systems and processes. You will be engaged in a wide range of interesting and challenging tasks.  

As a Principal Medical Writer  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be fully dedicated to a Top-5 pharmaceutical company. While working for our client, you will be able to profit from ICON through continued learning opportunities and building a longer-term career.