Remote Jobs at ICON plc
Find your next remote opportunity · 27 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 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.
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.
Regulatory Submissions Manager
Manager, Regulatory Affairs contributing to drug development as part of the Regulatory Affairs team at ICON plc. Providing regulatory guidance and operational support across various stages of drug development.
Patient Engagement Manager
Senior Patient Recruitment Lead managing clinical trial recruitment strategies at ICON. Collaborating with teams to enhance patient access and engagement through effective recruitment initiatives.
Manager, TMF
Manager, Trial Master File overseeing strategic and operational management of TMF across clinical studies at ICON plc. Ensuring compliance and providing end-to-end oversight for regulatory readiness.
Site Care Partner – Oncology
Site Care Partner overseeing oncology clinical research studies in Canada. Focused on site management and enrollment strategies to enhance operational effectiveness.
Clinical Research Site Project Manager
Project Manager leading single service clinical research projects at ICON’s Accellacare team. Ensuring project timelines, budgets, and quality while collaborating with cross-functional teams.
Clinical Outcomes Assessment Analyst
Clinical Outcomes Assessment Analyst developing reliable evidence for patients, regulators, physicians, and payers. Supporting clinical trial development and ensuring effective execution of research strategies.
Clinical Research Associate – Cross Therapeutic
Clinical Research Associate managing start-up activities for clinical trials at ICON. Collaborating with operations teams to ensure site qualification and compliance with regulatory standards.
Senior Statistical Programmer
Senior Statistical Programmer analyzing clinical trial data at ICON plc. Developing SAS programs and collaborating with biostatisticians to ensure high-quality results.
Clinical Research Associate, Multi TA
Clinical Research Associate overseeing trial site activations for ICON plc. Collaborating with teams to ensure compliant and timely initiation of clinical trials across various therapeutic areas.
Clinical Data Engineer
Senior Clinical Data Science Programmer developing programming solutions for clinical trial data analysis and reporting at ICON. Collaborating with data scientists and biostatisticians for effective data management.
Clinical Feasibility Analytics Manager
Feasibility Analytics Manager at ICON plc providing analytical services for clinical trial execution. Ensuring optimal planning and execution aligned with program strategies and timelines.