Remote Jobs at ICON plc
Find your next remote opportunity · 20 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 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.
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.
Supplier Performance Manager
Supplier Performance Manager at ICON plc managing supplier relationships and project coordination in healthcare. Contributing to clinical development through governance and standards implementation.
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.
Senior Biostatistician II
Senior Biostatistician II leading and overseeing clinical trials at ICON plc. Responsible for statistical components and client interactions in a healthcare research environment.
Clinical Trial Manager – Early Oncology
Clinical Trial Manager managing daily operations of early oncology trials at ICON plc. Ensuring compliance with GCP/ICH guidelines and driving project success.
Senior Clinical Research Associate – Midwest, Illinois/Michigan
Senior Clinical Research Associate at ICON plc overseeing clinical trials to ensure compliance and data integrity. Collaborating with teams and managing site activities in a diverse environment.
Senior Statistical Programmer
Senior Statistical Programmer analyzing clinical trial data and ensuring high-quality results at ICON plc. Collaborating to develop and validate statistical programs for clinical studies.
Statistical Programmer II
Statistical Programmer II at ICON responsible for developing and validating statistical programs for clinical trials. Collaborating with biostatisticians to ensure accurate implementation of analyses.
Congress Operations Specialist
Congress Planning Specialist managing sponsorships and corporate memberships for Global and Regional Congresses across disease areas at ICON plc. Supporting Congress project managers and maintaining department projects.
Local Trial Manager
Local Trial Manager managing clinical trial commitments and ensuring data quality in the US. Leading site selection, budget management, and compliance for ICON plc in clinical research.
Principal Medical Writer
Principal Medical Writer at ICON plc leading development of regulatory and clinical documents. Collaborating with cross-functional teams to ensure compliance and quality standards in clinical writing.
Senior Specialist, Publications Operations
Senior Site Management Associate overseeing site management activities for clinical trials at ICON plc. Collaborating with clinical teams to maintain regulatory compliance and high-quality data.
Statistical Programmer I
Statistical Programmer I developing and validating statistical programs for clinical trial analysis at ICON. Collaborating with teams to ensure data integrity and accurate reporting.
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