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...

Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical.    We are looking for an Global Study Manager/Associate Project Manager to join a growing and successful team working within Cardiovascular studies. This is a permanent and home-based role.    Countries we can...

Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical.    We are looking for an Global Study Manager/Associate Project Manager to join a growing and successful team working within Cardiovascular studies. This is a permanent and home-based role.    Countries we can...

Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical.    We are looking for an Global Study Manager/Associate Project Manager to join a growing and successful team working within Cardiovascular studies. This is a permanent and home-based role.    Countries we can...

Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical.    We are looking for an Global Study Manager/Associate Project Manager to join a growing and successful team working within Cardiovascular studies. This is a permanent and home-based role.    Countries we can...

Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical.    We are looking for an Global Study Manager/Associate Project Manager to join a growing and successful team working within Cardiovascular studies. This is a permanent and home-based role.    Countries we can...

As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   This position is responsible for the development of clinical documents for worldwide submissions to regulatory authorities.     Senior Medical Writer works directly with multidisciplinary project team members with the goal of independently writing...

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

Job Title: Clinical Research Associate (CRA) Location: Cape Town, South Africa Company: ICON Strategic Solutions – FSP

As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   As a Senior Medical Writer you will be supporting a Top-5 pharma company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. While being stably employed with ICON, you will be fully embedded with our client. 

As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Senior Clinical Scientist will support late phase development in oncology area, this role is dedicated to a global biotech company

As a Global (Senior) CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working location: ICON office, fully office based. **No flexible to work from home.

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 Patient and Engagement Specialist (Project Manager) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Patient & Site Engagement (PSE) Operations Specialist (OS) services provide the PSE Managers with administrative support for the management, execution and timely delivery of tactics for patient and site-facing initiatives in support of a clinical trial. Interface with key Delivery Unit customers Trial Delivery Leaders (TDLs),...

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.    For our client, a well-known global, pharmaceutical company we are looking for an experienced Clinical Research Associate

Are you ready to lead with impact in Pharmacovigilance? Join us as a PV Controlled Documents Professional  fully dedicated to one global pharmaceutical sponsor, and play a key role in ensuring data integrity and regulatory excellence in patient safety. IT IS A HYBRID ROLE WITH 3 DAYS IN THE CLIENT OFFICE IN WARSAW   - The Senior Manager Controlled Documents Professional is responsible for contributing to the development and implementation of the overall...

Are you ready to lead with impact in Pharmacovigilance? Join us as a PV Compliance Professional , fully dedicated to one global pharmaceutical sponsor, and play a key role in ensuring data integrity and regulatory excellence in patient safety. IT IS A HYBRID ROLE WITH 3 DAYS IN THE CLIENT OFFICE IN WARSAW - Perform PV Compliance related tasks systematically and effectively while complying with PV related local...

Job title:Study Start Up Manager  Location: UK (fully homebased) Fully sponsor dedicated   As a Study Start Up Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Statistical Programmer 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 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 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...