Site Management Associate

IRE

6d • Remote

About The Position

Global Study Associate (GSA) - LATAM ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency. Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Requirements

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
• Experience supporting in global clinical research, site management, or related administrative roles.
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
• Strong knowledge of clinical trial processes and regulatory requirements.
• Excellent communication and interpersonal skills, with the ability to work collaboratively within a Global team environment.
• Home Office Based in Brazil, Chile or Perú
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level