Study Delivery Specialist
ICON · Mexico City, Mexico
The apply link worked recently (not employer-confirmed).
Role summary
This home-based position in Mexico City involves supporting clinical trial site management and monitoring activities. Responsibilities include assisting with protocol compliance, documentation, data entry, and cross-functional communication while maintaining regulatory standards. The role requires a bachelor's degree in a life sciences or related field, clinical research experience preferred, and strong organizational and communication skills.
What they're looking for
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Strong organizational skills with meticulous attention to detail
- Knowledge of clinical trial processes and regulatory requirements
- Excellent written and verbal communication abilities
- Ability to collaborate effectively across cross-functional teams
- Willingness to travel approximately 25% as needed
What you'll be doing
- Assist with monitoring clinical trial sites for protocol adherence and GCP compliance
- Support site management including documentation preparation and data entry
- Collaborate with teams to address site-related issues and facilitate communication
- Maintain accurate records of site activities and contribute to monitoring reports
- Participate in training initiatives to build clinical trial management expertise
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.