Clinical Trial Coordinator

ICON Clinical Research; Santiago; Hybride; CLP 41 257 000 - 62 868 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance options

Retirement planning

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Résumé du poste

ICON Strategic Solutions in Santiago, Chile is seeking a Clinical Trial Coordinator to join our sponsor-dedicated team in a hybrid role. You will support site monitoring activities, ensure protocol compliance, and help maintain efficient trial operations.

You will collaborate with cross-functional teams, prepare documentation, enter data, and track site performance while traveling about 25% as required. A life sciences or clinical research background and strong organizational skills are

Qualifications

• Bachelor's degree in life sciences, healthcare administration, or clinical research.
• Experience in clinical research or site management preferred but not required.
• Strong organizational skills and ability to multitask.
• Basic knowledge of clinical trial processes and regulatory requirements is a plus.
• Excellent communication and teamwork.
• Willingness to travel ~25%.

Responsabilités

• Assisting in monitoring clinical trial sites and ensuring adherence to study protocols and GCP.
• Supporting site management activities, including documentation, data entry, and tracking site performance metrics.
• Collaborating with cross-functional teams to address site-related issues effectively.
• Maintaining accurate records of site activities and contributing to monitoring reports.
• Participating in training and development initiatives for trial management.

Connaissances

Organizational skills

Attention to detail

Communication skills

Team collaboration

Willingness to travel

Formation

Bachelor's degree in life sciences / healthcare / clinical research

Description du poste

Clinical Trial Coordinator - Hybrid - Santiago, Chile

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

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.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• 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.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

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

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

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

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

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

• Willingness to travel as required (approximately 25%)

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family's needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)