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

As a Sr. TAT (Targeted Alpha Therapeurics) Expert you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

The eCOA Operations Lead serves as a functional subject matter expert (SME) in the field of electronic Clinical Outcome Assessments (eCOA), driving process optimization, standardization, and operational excellence across clinical programs. This role collaborates closely with internal partners, such as Global Clinical Operations, Clinical Development, HEOR, Program Management, Quality, Legal and Regulatory Affairs, as well as external partners (CROs, eCOA Vendors, etc.) to enhance efficiency and effectiveness in eCOA implementation across the portfolio.  

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.

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

This Sr Trade Analyst within Global Clinical Supply Compliance Operations is responsible for ensuring imports/exports are declared and shipped in compliance with local Customs and other government agency regulations, Global Trade Compliance (GTC) standards, and post-entry auditing experience.   Individuals local to the PA/NJ/DE areas are preferred.   

This Sr Trade Analyst within Global Clinical Supply Compliance Operations is responsible for ensuring imports/exports are declared and shipped in compliance with local Customs and other government agency regulations, Global Trade Compliance (GTC) standards, and post-entry auditing experience.  

As a Clinical Study Lead 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.

As a Clinical Trial 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.

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

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

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

As a Senior Medical Director, Biotech 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.

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

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