Are you ready to lead with impact in Pharmacovigilance? Join us as a Manager, Data Assurance, 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   - Responsible for development and...

As a Medical Director you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Medical Director, Clinical Development Sciences Hematology may lead the clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contributes to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for 1 program, leading the...

As an Associate Project manager at ICON, you will play a pivotal role in supporting the coordination and management of clinical trials, contributing to the design, analysis, and advancement of treatments and therapies.

Principal CRA (Lead CRA Role), Home-Based, Bangkok Thailand   As a (Principal CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Clinical Trial Manager - (Vaccines) - Home-based, South Korea   As a (Clinical Trial Manager) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

We are hiring a Clinical Trial Manager, sponsor dedicated (Eindhoven area)Position Summary: The Clinical Trial  Manager plays a key role in ensuring high-quality clinical study execution across all active clinical research initiatives. You will lead, support, and manage clinical studies to generate critical clinical evidence, aligned with business goals and regulatory compliance requirements. The role requires close collaboration with cross-functional teams, effective use of...

As a SMA I, 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.    For our client, a well-known global, pharmaceutical company we are looking for an experienced Clinical Research Associate to work on fast-paced studies in...

🚀 Op zoek naar een nieuwe uitdaging als CRA?   Werken voor één sponsor en toch blijven groeien? 👉 Dan is dit jouw kans! ICON plc is op zoek naar een ervaren Clinical Research Associate (CRA). Samen bepalen we welk level het...

Vacature: Start-Up Manager Klinische Studies – Jouw Kickstart voor Succes! Ben jij een ervaren Clinical Research Associate of een doorgewinterde professional die houdt van het organiseren en laten draaien van klinische studies? Heb jij oog voor detail, gevoel voor financiën en weet je als geen ander hoe je een klinisch onderzoek vliegend van de grond krijgt? Dan zoeken wij jou!  

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

We currently have an exciting new opportunity for an experienced Global Clinical Project Manager within the Oncology team to join a successful sponsor dedicated program. We are looking for a Global Clinical Project Manager which is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the project delivery of clinical studies.   The Global Clinical Project Manager is responsible for leading a cross-functional study team and for providing the team with direction and guidance to enable...

As a Clinical Development Scientist  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   At this role you will lead a clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contribute to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for one or several projects,...

As a Sr. 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 a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work in a...

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.

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.

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 a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work in a...

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

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

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.