Site Management Associate II (Remote CRA II)

Site Management Associate II (Remote CRA II) - Homebased - Brazil or Mexico

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.

We are currently seeking a Site Management Associate II to join our diverse and dynamic team. As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel.

What You Will Be Doing:

• Conducting remote and risk-based monitoring activities for clinical trials across multiple therapeutic areas.
• Supporting site qualification, initiation, monitoring, and close-out activities in collaboration with study teams.
• Ensuring protocol compliance, data integrity, and patient safety throughout the clinical trial process.
• Performing remote data review, query management, and source documentation reconciliation to maintain high-quality clinical data.
• Building strong relationships with investigators and site staff to support smooth study execution and issue resolution.
• Reviewing study metrics, identifying potential site risks, and proactively escalating concerns when appropriate.
• Contributing to the preparation and review of study documentation, including protocols, monitoring plans, and clinical study reports.
• Supporting a highly remote monitoring model with occasional travel requirements depending on business needs.

Your Profile:

• Bachelor’s degree in a scientific or healthcare-related field.
• Minimum of 2 years of clinical research monitoring experience.
• Strong understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Previous monitoring experience in Brazil or Mexico is required; exposure to studies in the U.S. or Canada is considered a plus.
• Excellent organizational, communication, and relationship-management skills with strong attention to detail.
• Ability to work independently and collaboratively within a fast-paced global environment.
• Comfortable working in a highly remote operational model with virtual collaboration across international teams.
• Valid U.S. visa is required, as occasional international travel may be required based on study or business needs.
• Advanced English communication skills is needed.

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply