Remote Jobs at ICON plc
Find your next remote opportunity · 28 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.
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.
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.
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.
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.
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.
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 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.
Clinical Research Associate – FSP
Clinical Research Associate II at ICON conducting clinical trial monitoring and analysis. Collaborating with site staff and maintaining high-quality clinical data while ensuring compliance.
Logistics Coordinator II
Logistics Coordinator II managing logistics operations for clinical trials at ICON plc. Overseeing shipments, deliveries, and inventory management to enhance supply chain performance.
Site Payment Analyst
Site Payments Specialist managing site payments and subject reimbursements for clinical studies at ICON, a leader in healthcare intelligence and clinical research. Collaborating with vendors and stakeholders to ensure accurate payment processing.
Senior Associate Study Manager
Senior Associate Study Manager supporting clinical studies execution and monitoring at ICON plc, a clinical research organization. Collaborates on study planning, site management, and vendor relationships.