Site Engagement Study Manager
ICON · Mexico City, Mexico
The apply link worked recently (not employer-confirmed).
Role summary
This home-based position involves overseeing day-to-day clinical trial operations across multiple sites, coordinating cross-functional teams through study phases from start-up to close-out. The role requires managing timelines, budgets, and regulatory compliance while serving as the operational liaison with sponsors and developing site engagement strategies. Candidates need 2–5 years of clinical trial experience, familiarity with GCP standards, and proficiency managing stakeholders in matrix environments.
What they're looking for
- Bachelor's degree in relevant discipline
- 2-5 years clinical trial operations experience with site engagement exposure
- Strong clinical study or project management background in CRO, pharma, or biotech
- Solid understanding of GCP, clinical trial operations, and regulatory requirements
- Proven cross-functional team coordination and multi-stakeholder management skills
- Experience with global, multi-country trials and matrix environments
- Advanced English proficiency
What you'll be doing
- Manage planning, execution, and close-out of clinical studies per protocol and ICH-GCP standards
- Lead cross-functional teams coordinating start-up, enrollment, monitoring, and data cleaning activities
- Serve as primary operational contact for sponsors with regular status updates and expectation management
- Develop site engagement plans including country/site strategies, cadence, and escalation triggers
- Track and drive completion of actions across teams ensuring accountability and timely execution
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.