We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate 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.

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.

Investigator Contracts Lead is responsible for direct site-facing contract and budget negotiations thought contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. 

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.

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

We are currently seeking a Senior Medical Director to join our diverse and dynamic team. As a Senior Medical Director at ICON, you will play a pivotal role in leading the medical strategy and oversight of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.

CTA Line Manager needed  for a 1-year contract(maternity leave cover), office-based in Cambridge, UK!   We are looking to recruit a CTA Line Manager with solid CTA experience and some management experience.   This is a 1-year contract to start as soon as possible, to enable the successful candidate to...

Driving clinical trial excellence through operational and administrative support   As a key member of the Local and Global Study Teams, the CTA ensures seamless coordination of global Phase I–IV clinical trials. Working within GCP, regulatory, and company guidelines, this role supports the delivery of high-quality data for regulatory approvals.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate 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.

The Study Start Up Associate fulfills the role of Local Regulatory Affairs Lead (LRAL) and is responsible for preparing, submitting and following up on initial and amended Regulatory Agency (RA), Central Independent Ethics Committee (IEC), and any other central submissions required in the country(s) they are responsible for, within contracted timelines and budget, in accordance with local regulatory requirements and sound scientific/technical principles, including the creation and modification of documentation required for approval.

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Role: Clinical Research Physician - Inflammation & Autoimmunity (FSP), part-time (0.5 FTE)  Location: Australia (home-based)   We are seeking an experienced Clinical Research Physician to provide medical monitoring and scientific oversight for clinical trials in inflammation and autoimmunity. This role offers the opportunity to work on innovative programs,...

We are currently seeking a Senior Manager, Pharmacovigilance to join our diverse and dynamic team. As the Senior Manager in this role at ICON, you will be responsible for overseeing pharmacovigilance activities to ensure the safety and efficacy of our clinical trials. Your leadership will be critical in maintaining compliance with regulatory requirements and enhancing the overall safety monitoring processes across the organization. - Pharmacovigilance responsibilities may include both clinical trial phases and post-marketing surveillance. -

As a Senior Clinical Trial Manager (Client title: Project Manager) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

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

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.

As a Global Clinical Project Specialist 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. Identify, select, initiate and closeout appropriate investigational sites for clinical studies. • Monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with ICON SOPs/WPs applicable regulations and the principles of ICH-GCP.

Project Manager, Home-based, South Korea   As a (Project Manager) 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...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.