Site Specialist II
ICON · Lima, Peru +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Site Specialist II manages clinical trial site operations and regulatory documentation for ICON, a global clinical research organization. The role involves coordinating site support activities, maintaining regulatory compliance, and facilitating study start-up across assigned sites in Peru and Argentina.
What they're looking for
- Bachelor's degree in life sciences, healthcare, or related field
- Minimum 2 years clinical research or regulatory affairs experience
- Experience with study start-up activities and regulatory submissions
- Strong knowledge of ICH-GCP and local regulatory requirements
- Fluency in English and Spanish
- Excellent organizational and project management abilities
What you'll be doing
- Coordinate document collection, review, and maintenance for assigned sites ensuring compliance
- Serve as operational liaison for site staff on documentation, systems, and process questions
- Prepare and submit regulatory documents including trial applications and ethics committee submissions
- Support planning and logistics for site meetings, investigator meetings, and monitoring visits
- Identify and contribute to site workflow improvements and process optimization initiatives
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.