Central Study Coordinator (Medtech)

TL;DR

Central Study Coordinator (Medtech): Coordination and support of remote site activities for assigned projects with an accent on site communications, recruitment, and regulatory compliance. Focus on maintaining documentation according to IRB/FDA policies and managing clinical databases.

Location: Must reside in Mexico

Company

hirify.global provides customizable consulting solutions to biotech, med device, and pharmaceutical organizations to accelerate the advancement of scientific breakthroughs.

What you will do

• Serve as the primary point of contact for daily site communications, document submissions, and activity coordination.
• Support recruitment, pre-screening, and screening activities as assigned.
• Manage subject re-consenting, acquire medical records, and conduct protocol activities.
• Perform data entry, monitor clinical databases, and resolve system queries.
• Maintain study documentation in strict compliance with IRB and FDA policies.
• Assist with study closeout and other site-related operational activities.

Requirements

• Bachelor's degree or a minimum of 2 years of related combined experience.
• Must reside in Mexico.
• Current knowledge and ability to apply ICH / GCP regulations and guidelines.
• Competence in applying standard business procedures and SOPs.
• Strong verbal and written communication skills.
• Ability to manage technology and web-based research platforms in a remote workspace.

Culture & Benefits

• Remote-first work approach with support for remote working.
• Strong commitment to diversity, equity, and inclusion.
• Collaborative and entrepreneurial work environment.
• Human-centric hiring process with personal review of all applications.