Remote Jobs at ICON plc
Find your next remote opportunity · 48 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 II – Senior Clinical Research Associate
Clinical Research Associate monitoring clinical trials at ICON Plc, interpreting medical data and ensuring protocol compliance. Collaborating with site staff to facilitate smooth study conduct.
Study Manager
Study Manager supporting operational conduct of clinical studies in ophthalmology. Collaborating with teams and managing timelines for clinical drug development.
Investigator Contracts Lead, Contract Analyst II
Contract Analyst II at ICON analyzing contracts and clinical trial data. Collaborating on regulatory compliance and contract management in the healthcare sector.
Clinical Research Associate
CRA II at ICON designing and analyzing clinical trials while ensuring protocol compliance and data integrity. Collaborating with investigators and site staff for smooth study conduct in clinical trials.
Senior Contract Analyst
Senior Contract Analyst managing contractual agreements to ensure compliance for clinical research at ICON. Collaborating with stakeholders and supporting project teams to optimize contract processes.
Clinical Research Associate
Clinical Research Associate conducting monitoring visits and managing clinical site quality for ICON. Ensuring protocol compliance and collaborating with investigators in clinical trials.
Clinical Scientist
Clinical Scientist role at ICON supporting respiratory clinical studies with interaction with various stakeholders. Work involves medical monitoring and data management responsibilities.
Senior Clinical Data Science Lead
Lead the clinical data management and analysis at ICON, enhancing digital health data for clinical trials. Oversee project deliverables while collaborating with cross-functional teams.
Clinical Scientist I
Clinical Scientist conducting studies to advance understanding of new therapies at ICON plc. Designing protocols and collaborating with teams to ensure quality and efficiency.
Clinical Trial Manager
Clinical Trial Manager managing clinical trial operations at ICON plc. Oversee clinical trials while ensuring compliance with regulations and quality standards.
Senior Global Project Manager
Senior Project Manager at ICON managing global clinical projects with a focus on Oncology. Leading projects and teams while ensuring successful delivery and strategic planning.
Payment Analyst
Grants Specialist at ICON responsible for grant application management and compliance. Collaborating with stakeholders to develop compelling proposals for clinical development.
Senior Regulatory Publishing Associate
Senior Regulatory Ops Associate overseeing regulatory document management for clinical trials at ICON healthcare intelligence. Collaborating cross-functionally to optimize regulatory processes for innovative therapies.
Project Manager, Feasibility Site Activation
Project Manager overseeing global clinical study start-up strategies at ICON. Leading cross-functional collaboration for effective regulatory and contract execution across participating countries.
Clinical Research Associate
Clinical Research Associate overseeing clinical trial activities at ICON plc. Ensuring compliance, data integrity, and participant safety during clinical trials.
Project Manager
Project Manager overseeing project delivery and team leadership at ICON plc, a world-leading clinical research organization. Focused on timelines, budgets, and communication with stakeholders.
Site Budgeting and Contracting Specialist
Contract Analyst I at ICON preparing invoicing and managing client relationships. Responsible for electronic processing and reconciliation of accounts in clinical research.
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.
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.
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.