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

📌 Sma i (Ciudad de México)
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📍 Ciudad de México