Mexico. Home based.

ICON is a integral 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 Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include

- Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
- Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.




- Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
- Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.

Your Profile: You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required qualifications and experience

- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
- Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
- Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
- Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
- Willingness to travel as required (approximately 60%)

📌 Clinical Associate (México)
🏢 Icon Clinical Research
📍 México