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 Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through centralized monitoring activities, contributing to the advancement of innovative treatments and therapies.
What You Will Do
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities Include
Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality.
Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities and implement corrective and preventive actions as necessary.
Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes.
Provide support and guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements.
Contribute to the development and optimization of centralized monitoring strategies and protocols to maximize data quality and compliance across clinical trials.
Your Profile
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required Qualifications And Experience
Bachelor's degree in life sciences, computer science, or a related discipline
Previous experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO industry.
Strong understanding of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA regulations).
Excellent analytical and critical thinking skills with the ability to iden
📌 Central Monitor (México)
🏢 ICON Strategic Solutions
📍 México
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