A Clinical Research Associate 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 be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

A Clinical Research Associate 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 be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

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.

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.

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...

As a Medical Data Reviewer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will have the opportunity to gain experience working with a large biotech company, a pioneer and industry leader in the area of Antibody research, that utilizes their innovative technology platform across multiple therapeutics areas like Oncology,...

Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team, for pharmaceutical and biotechnology company company partner.   You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

A Clinical Research Associate 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 be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

Site Management Associate Location: Bangalore    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.

This is an unique opportunity to join an exciting embedded sponsor team as Site Management Associate (SMA) in ICON Bangalore office. The SMA is accountable end to end from commit to study initiation until study archiving from planning and leading the delivery of interventional, studies to time, quality, budget, company standards and scientific requirements as outlined in the clinical study proposal.      Key Responsibilities:

As a Site Management Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will provide support to the clinical trial team at the global level impacting directly project's success

As a Study delivery specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Senior Clinical Data Coordinator (Sr CDC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   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.

As a Global Professional Event Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be responsible for the end to end planning and execution of global engagement programs, including medical education, advisory boards, expert input forums, Consulting Service Agreements (CSAs) and scientific input engagements.

Role: CRA II Location: Sydney/ Australia (hybrid - working from home and from the sponsor office during onboarding)   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 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.