Remote Jobs at ICON plc
Find your next remote opportunity · 34 Open Positions
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries.
We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Clinical Site Manager II
Senior Clinical Research Associate overseeing and managing clinical trial activities for ICON Plc. Ensuring compliance with regulatory requirements and industry standards while supporting successful trial execution.
Project Manager
Project Manager leading and coordinating project activities in a world-leading healthcare research organization. Ensuring projects are delivered on time and within budget for ICON.
Manager, Clinical Operations II / Clinical Study Manager II
Join ICON as a Clinical Trial Manager II, contributing to the design and analysis of clinical trials. Collaborate with cross-functional teams to enhance innovative treatments and therapies.
Site Activation Partner
Study Start Up Associate I role facilitating clinical trial initiation and ensuring regulatory compliance at ICON plc. Join a leading healthcare intelligence and clinical research organization with a commitment to inclusion and excellence.
In-House Clinical Research Associate
In-House Clinical Research Associate at ICON plc supporting the execution and management of clinical trials. Contributing to innovative treatments and therapies.
Clinical Trial Specialist
Senior Site Management Associate ensuring compliance and data quality in clinical trials for ICON. Overseeing site management activities and mentoring junior staff for effective collaboration.
Senior Clinical System Designer, Sponsor Dedicated
Senior Clinical System Designer designing and analyzing clinical trials at ICON plc. Contributing to the advancement of innovative treatments and therapies within a diverse team.
Senior Clinical System Designer
Senior Clinical System Designer at ICON leading clinical trial design and analyzing medical data. Collaborating with teams on innovative treatments and therapies.
Senior CRA / CSM
Senior Clinical Research Associate overseeing clinical trial activities at ICON plc to ensure protocol compliance. Contributing to the success of clinical trials by ensuring data integrity and participant safety.
Principal Statistical Programmer
Principal Statistical Programmer at ICON plc leading SAS programming for clinical research. Influencing study strategy and ensuring data integrity in a remote environment.
Project Manager
Project Manager at ICON leading and coordinating project activities in clinical development. Ensuring delivery on time and quality standards across cross-functional teams.
Clinical Trial Manager, Senior Clinical Trial Manager
Project Manager at ICON plc overseeing clinical trial projects, ensuring delivery on time and within budget. Leading cross-functional teams and engaging with stakeholders across project execution.
Senior Clinical Project Manager, Quality
Senior Clinical Project Manager at ICON, leading projects in clinical development and ensuring successful execution. Collaborating with cross-functional teams and stakeholders to achieve project objectives.
Clinical Site Manager II – Sr CRA
Senior Clinical Research Associate at ICON plc, overseeing clinical trial activities and ensuring compliance with protocols. Collaborating with teams and managing site performance to ensure successful execution.
Clinical Site Manager II – Senior CRA
Senior Clinical Research Associate overseeing clinical trial activities for ICON plc. Ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
Associate Director, Clinical Data Manager
Associate Director leading clinical data management and oversight of CROs for global trials at ICON plc. Fostering innovative environments and ensuring compliance in R&D financial standards.
Senior Programmer
Statistical Programmer II developing statistical programs for clinical trials at ICON. Collaborating with teams to ensure regulatory compliance and data integrity in research projects.
Senior Contract Analyst
Senior Contract Analyst at ICON managing contracts and compliance for clinical research projects. Collaborating with stakeholders and contributing to innovative treatments in an inclusive environment.
Regulatory Submissions Manager – EU CTR
Regulatory Affairs Manager at ICON overseeing submissions across EU and UK for drug development. Leading regulatory activities and providing support within a cross-functional team environment.
Senior Regional Pharmacovigilance Manager
Senior Manager in Pharmacovigilance at ICON ensuring compliance and leading safety monitoring processes. Collaborate regionally and drive continuous improvement initiatives in drug safety.