Study Management Associate III (Clinical Research)

Location: Mexico City, Mexico; global role that may be located virtually

Company

hirify.global develops medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Lead and contribute to one or more global Phase 0–4 clinical trials from inception through closure.
• Support cross-functional study strategy, stakeholder engagement, meeting facilitation, documentation, and delivery tracking.
• Manage external vendors, including RFPs, vendor selection, scopes of work, deliverables, and risk management.
• Develop and execute global recruitment strategies, mitigation plans, and retention activities.
• Manage study materials, CTMS and eTMF records, inspection readiness, and risk identification and escalation.
• Support EDC, IRT, and ePRO design, testing, access, query resolution, investigational product management, training, and process improvement.

Requirements

• Bachelor's degree.
• At least 4 years of progressive pharmaceutical or clinical research experience.
• Knowledge of SOPs, ICH/GCP, global regulations, and quality procedures.
• Experience using EDC, IRT, CTMS, and eTMF systems.
• Strong analytical, critical-thinking, organizational, and time-management skills.
• Proficient business and technical English, both oral and written.

Nice to have

• Experience across study initiation through completion.
• Global study experience.

Culture & Benefits

• Work in a cross-functional global study management team.
• Operate in a fast-paced environment with opportunities to work independently and collaboratively.
• Participate in mentoring, subject-matter-expert activities, and process improvement initiatives.