About the role

Senior Clinical Trial Associate supporting the management and execution of clinical trials at ICON Plc. Handling administrative tasks and monitoring trial operations for successful project outcomes.

Responsibilities

Support the management and execution of clinical trials by handling a range of administrative and operational tasks
Provide administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records
Assist in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements
Collaborate with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study
Monitor and track trial progress, including managing site communications and ensuring timely delivery of study materials
Build and maintain strong relationships with site staff and other stakeholders to facilitate smooth trial operations

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements
Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively
Proficiency in clinical trial management systems and relevant software
Excellent communication, interpersonal, and problem-solving skills
Willingness to travel as required (approximately 10%)

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways