Support clinical trial site management and monitoring activities in a remote role based in Mexico City. Assist with protocol compliance, documentation, and cross-functional coordination while contributing to high-quality clinical research delivery.
Responsibilities
Assist with monitoring of clinical trial sites for protocol adherence and GCP compliance
Support site management activities including documentation preparation and data entry
Maintain records of site activities and contribute to monitoring report preparation
Collaborate with cross-functional teams to address site-related issues and facilitate communication
Participate in training initiatives to develop clinical trial management knowledge and skills
Requirements
Bachelor's degree in life sciences, healthcare administration, or clinical research
Strong organizational skills and attention to detail with multitasking ability
Excellent communication and interpersonal skills for team collaboration
Basic knowledge of clinical trial processes and regulatory requirements
Willingness to travel approximately 25% as required
Some clinical research, site management, or related administrative experience preferred

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