RBQM Manager leading implementation of risk management strategies throughout clinical trial lifecycle. Working with global teams to drive quality oversight and regulatory compliance in clinical development.
IP
ICON plc
Currently Hiring
About the company
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.
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125 jobs found
Senior Regulatory Scientist providing regulatory and scientific expertise for global clinical development at ICON. Leading strategy development, authoring documents, and mentoring staff.
Senior Clinical Data Science Lead overseeing analysis, interpretation, and management of clinical data initiatives at ICON. Driving success in clinical trials through leadership and data quality assurance.
Centralized Clinical Trial Manager at ICON responsible for reviewing clinical trial site visit reports and ensuring quality standards. Act as a liaison for timely resolution of issues.
Senior Regulatory Scientist at ICON providing expertise to support global clinical development strategies and submissions. Navigating regulatory landscapes to enable successful program execution.
HR Manager leading benefits operations for ICON, a healthcare intelligence organization. Managing team performance and overseeing benefits administration for US and Canada employees.
Data & Reporting Analyst II at ICON focusing on master data management and providing insights. Collaborate with teams to improve data quality and support business objectives while working in a hybrid environment.
Site Partner II coordinating site activations and maintaining communication with stakeholders for clinical studies. Responsible for ensuring timely approval and quality of site documentation.
Senior Clinical Trial Manager at ICON driving clinical trial management and delivery of clinical study objectives in healthcare intelligence.
Senior Clinical Research Associate overseeing clinical trial activities at ICON plc. Ensuring data integrity and compliance throughout the study lifecycle with various responsibilities.
Clinical Data Configuration Engineer at ICON shaping the future of clinical development. Driving data ingestion, configuration, and collaborating with engineering teams in clinical trials.
Manager of Clinical Systems overseeing system implementation at ICON, a healthcare intelligence firm. Responsible for optimizing clinical systems to support trial management and data integrity.