Site Management Associate

ICON; Ciudad de México; Presencial; MXN 480,000 - 600,000; Jornada completa

Descripción de la vacante

A leading healthcare intelligence organization is seeking a Senior Clinical Trial Associate to support clinical trials in Mexico. This role involves administrative support, document management, and collaboration with cross-functional teams to ensure successful trial execution. Candidates should possess an advanced degree in a relevant field along with over 2 years of clinical trial experience. The position offers a competitive salary and diverse benefits focused on well-being and work-life balance, making it an excellent opportunity for professionals in the field.

Servicios

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Flexible optional benefits

Formación

• Min 2+ years of experience in a clinical trial support role.
• Solid understanding of clinical trial processes and regulatory requirements.
• Ability to manage multiple tasks and projects effectively.

Responsabilidades

• Provide administrative support for clinical trials.
• Assist in the preparation and submission of regulatory documents.
• Collaborate with cross-functional teams to support trial operations.

Conocimientos

Strong organizational skills

Excellent communication skills

Proficiency in clinical trial management systems

Detail-oriented

Interpersonal skills

Educación

Advanced degree or certification in life sciences, healthcare, or clinical research

Descripción del empleo

Senior CTA - Mexico - Dedicated sponsor role

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Senior Clinical Trial Associate (CTA) to join our diverse and dynamic team, supporting a dedicated sponsor. As a Senior CTA you will play a key role in supporting the management and execution of clinical trials by handling a range of administrative and operational tasks. You will contribute to the smooth execution of clinical trials through efficient coordination, documentation, and communication with various stakeholders.

What You Will Be Doing:

• Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial‑related records.
• Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
• Collaborating with cross‑functional teams to support trial operations and resolve any issues that arise during the course of the study.
• Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
• Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile:

• Advanced degree or certification in a relevant field such as life sciences, healthcare, or clinical research.
• Min 2+ years of 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, with a keen eye for detail in documentation and data management.
• Excellent communication, interpersonal, and problem‑solving skills, with the ability to work collaboratively with diverse teams and stakeholders.

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 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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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