Clinical Trial Coordinator

ICON Strategic Solutions is hiring a Clinical Trial Coordinator to support clinical trial site management in a sponsor-dedicated model. The role assists with site monitoring, protocol and regulatory compliance, documentation, data entry, performance tracking, and monitoring reports.

Responsibilities

Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines

Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics

Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively

Maintaining accurate records of site activities and contributing to the preparation of monitoring reports

Participating in training and development initiatives to enhance knowledge and skills in clinical trial management

Preferred

Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory

Basic knowledge of clinical trial processes and regulatory requirements is a plus

Site Management

Administrative Experience

Clinical Trial Processes

Regulatory Requirements

Benefits

Remote work

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

Company

Outsourced clinical development and commercialization services for life sciences

Dublin , GB

https://www.iconplc.com/services/strategic-solutions/

10001+ employees

Qualifications

Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research

Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively

Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment

Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory

Basic knowledge of clinical trial processes and regulatory requirements is a plus

Required skills

Clinical Research, Site Management, Clinical Trial Processes, Regulatory Requirements

Experience

Entry level