Search the 21 jobs at ICON plc

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.

The Site Identification Specialist I role involves working closely with the Site Identification Functional Lead to identify potential clinical study sites across Germany, focusing on understanding the local healthcare system and building relationships within that context.

As an HR Advisor, you will provide essential HR support services, addressing inquiries and offering guidance on HR processes during the employee lifecycle. Collaborate with HR Managers to resolve issues and ensure alignment with service levels, contributing to an inclusive and collaborative culture.

As a Clinical Research Associate at ICON, you will oversee and coordinate clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data. You will also develop relationships with stakeholders and maintain documentation for studies while ensuring patient safety.

As a Statistical Programmer II, you will be responsible for the statistical aspects of clinical and preclinical research projects, including study design, analysis planning, and data reporting. You will develop and document SAS programs, assist in protocol implementation, and support statisticians in their tasks while coordinating analysis efforts across multiple projects.

As a Clinical Research Associate II, you will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring compliance and patient safety. You'll collaborate with site staff, resolve data queries, and prepare study documentation to maintain high-quality clinical data.

As a Senior Clinical Research Associate, you will coordinate activities for clinical studies, ensuring compliance with ICH-GCP guidelines. Responsibilities include monitoring study progress, submitting necessary documents for ethics approval, preparing regulatory submissions, and possibly mentoring junior CRAs. The role involves travel for site monitoring and requires strong communication skills.

As a Clinical Research Associate II Specialist, you will conduct site visits for clinical trials, ensure compliance and data integrity, collaborate with staff, resolve data queries, and prepare study documentation. This role is pivotal in advancing innovative medical treatments.

As a Clinical Research Associate at ICON, responsibilities include setting up and monitoring studies, completing reports, submitting documents for approvals, and ensuring study cost efficiency. Requires at least 12 months of monitoring experience in clinical trials and a college degree in medicine or science.

As an HR Manager, you will oversee HR Consulting Services across multiple countries, collaborating with leadership on HR strategies, labor law compliance, and employee relations. Your role includes managing case advice, implementing HR initiatives, and analyzing HR data to drive improvements.

As a Senior Clinical Research Associate at ICON, you will independently coordinate and monitor clinical trials, ensuring compliance with regulations and preparing documentation. You will manage site activities, submit protocols for IRB approval, mentor junior CRAs, and balance sponsor queries while maintaining accurate status reports. Extensive travel is required for site monitoring.