ICON seeks a Site Management Associate I in Mexico City to support clinical trial site operations. The role involves assisting with site monitoring, ensuring protocol compliance, managing documentation, and collaborating with cross-functional teams to maintain operational standards.
Responsibilities
Assist with monitoring of clinical trial sites for protocol adherence and GCP compliance
Support site management activities including documentation and data entry
Collaborate with cross-functional teams to address site-related issues
Maintain accurate records of site activities and contribute to monitoring reports
Participate in training initiatives to develop clinical trial management knowledge
Requirements
Bachelor's degree in life sciences, healthcare administration, or clinical research
Experience in clinical research, site management, or related administrative roles preferred
Strong organizational skills and attention to detail
Knowledge of clinical trial processes and regulatory requirements
Excellent communication and interpersonal skills
Willingness to travel approximately 25%

📌 Sma I (Xico)
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📍 Xico