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As a Study Start Up Associate II, you will lead the preparation and submission of regulatory documents, coordinate with stakeholders for study initiation approvals, manage regulatory compliance records, and support study teams on best practices while participating in process improvements.
As a Clinical Research Associate II, you will monitor general medicine trials, ensuring compliance with regulations by coordinating activities, preparing documentation, and mentoring less experienced CRAs. The role involves traveling for site monitoring and maintaining study records in a fast-paced environment.
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
The role involves familiarizing with ICON’s SOPs and ICH GCP guidelines, maintaining data accuracy, serving as a contact for study sites and investigators, conducting site management activities, and managing various study-related tasks. Excellent communication and organization skills are required along with travel flexibility.
The Study Start Up Associate II at ICON plc supports the initiation of clinical trials by evaluating feasibility, identifying trial sites, negotiating contracts, and ensuring regulatory compliance while contributing to patient safety and informed consent processes.
The Senior Study Start Up Associate will support study startup teams in large, fast-paced environments, ensuring efficient initiation of clinical trials by assessing feasibility, identifying sites, and negotiating contracts. Responsibilities also include providing expertise, ensuring regulatory compliance, and protecting patient welfare through informed consent processes.
The Senior Project Manager will oversee clinical trial project management, including stakeholder management, progress tracking, risk management, and coordination with various teams. They will ensure adherence to client agreements regarding timelines, quality, and costs, while providing guidance to junior team members.
As an HR Advisor at ICON, you will provide HR-related support to domestic employees, respond to inquiries, assist in recruitment processes, and guide on HR policies. You will enhance HR operations, maintain communication with Country HR Manager, and promote standardization and improvements in daily operations.
The IHCRA will support the planning, initiation, and execution of clinical trials. Responsibilities include assessing site feasibility, ensuring compliance with protocols and regulations, monitoring trial progress and data collection, and assisting in the preparation and review of trial documentation.
The Bacteriophage Therapeutics Research Technician II conducts research on phage therapeutics for microbial pathogens, develops phage cocktails for treatment, performs various assays, analyzes experimental results, and maintains laboratory operations and records.
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