Mexico. Remote.
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.
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. Working as a Clinical Study Assistant, exclusively assigned to a Pharmaceutical Company, you will perform tasks related to the planning and execution of clinical studies.
Key responsibilities include:
Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with established protocols under the general supervision of the Functional Service Provider (FSP) Manager and in collaboration with the CTA Manager(s)
Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model
Perform departmental tasks as needed
Accountabilities:
Review of study documentation, including essential document packets, study plans, informed consent forms
Supporting/oversight of risk-based monitoring
Attendance of key team meetings as required, including Minutes for selected studies
Supporting regulatory inspection readiness (e.g. SOP Lists, storyboard collation)
Support clinical trial systems (e.g. CTMS/TMF) and associated activities for selected studies
Supporting vendor contract administration as required
Support study close-out activities, e.g. financial reconciliation
Supporting additional ad-hoc activities as needed,



as agreed with Manager(s)
Collaboration with internal departments (Legal, Insurance, R&D; functions, etc.), CROs, and external vendors
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 scientific or healthcare-related field or equivalent international degree required
1-2 years' experience in pharmaceutical industry, clinical research organization, or related role
Experience in Phase 2 and 3 studies and global/international studies is advantageous
Experience working across multiple therapeutic areas (including oncology) is advantageous
Knowledge in global/regional regulatory and compliance requirements for clinical research
Demonstrated excellence in task management and cross-functional collaboration
Excellent communication skills
Excellent teamwork, organizational, interpersonal, and problem-solving skills
Fluent business English (oral and written)
Ability to work collaboratively in a fast-paced environment with attention to detail
Willingness to travel as required (approximately 10%)
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 integral 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

📌 Clinical Study Assistant (Xico)
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