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 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:
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials,
such as informed consent forms and case report forms.
- Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contribute to the tracking and reporting of clinical trial metrics and milestones.
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.:
- Experience in clinical research, with exposure to regulatory affairs, study start-up, or clinical trial documentation preferred.:
- Knowledge of Mexican regulatory requirements for clinical research, including COFEPRIS submissions and applicable local regulations.:
- Familiarity with ICH-GCP guidelines and clinical trial start-up processes.:
- Availability to work in a hybrid environment, including attendance at the office a couple of times per week.:
Employment with ICO
📌 Clinical Trial Associate (Ciudad de México)
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📍 Ciudad de México
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