Site Activation Lead - Clinical Trials (Hybrid)

ICON Clinical Research; Ciudad de México; Hybrid; MXN 650,000 - 900,000; Full time

Job summary

ICON Strategic Solutions, part of ICON, is seeking a Hybrid position in Mexico City for a Site Start-Up Coordinator. You will coordinate site start-up and activation, resolve issues, and develop team capability, supporting regulatory submissions across the US and Canada.

Fluency in English is required and experience with CTMS/eTMF is valued. Join a sponsor-dedicated model with ICON’s global expertise, contributing to trials that help patients worldwide.

Qualifications

• Site start-up experience in sponsor or CRO roles.
• Strong knowledge of ICH GCP and ethics requirements.
• Experience with US and Canada regulatory submissions.
• Fluency in English required.

Responsibilities

• Coordinate site start-up and activation delivery.
• Collect, review, QC, and file essential documents for submission.
• Review ICF changes and manage amendments.
• Ensure REB submissions are complete and activation-ready.
• Support regulatory start-up activities across US and Canada, including submission workflows.
• Maintain CTMS/eTMF documentation and timelines.

Skills

Site start-up

Regulatory submissions

IRB/REB knowledge

ICH GCP

English fluency

Cross-functional collab

Tools

CTMS

eTMF

Job description

ICON Strategic Solutions, part of ICON, is seeking a Hybrid position in Mexico City for a Site Start-Up Coordinator. You will coordinate site start-up and activation, resolve issues, and develop team capability, supporting regulatory submissions across the US and Canada.

Fluency in English is required and experience with CTMS/eTMF is valued. Join a sponsor-dedicated model with ICON’s global expertise, contributing to trials that help patients worldwide.