Interactive Response Technology (IRT) Implementation Analyst (Clinical Supply)

Location: Hybrid in Makati City, Philippines. The role requires periodic meetings with global teams from 8:00 p.m. to 5:00 a.m. or 9:00 p.m. to 6:00 a.m. Philippine Time.

Company

hirify.global develops and delivers medicines while managing clinical supply strategies and investigational medicinal products for global clinical research trials.

What you will do

• Support IRT configuration, testing, and delivery plans for new and amended clinical studies.
• Elicit and document system requirements with study teams and support the design and configuration of study builds.
• Support the development and execution of User Acceptance Testing plans.
• Coordinate meetings, capture minutes, prepare IRT support documents, and deliver investigator meeting slides.
• Help resolve study and system issues, including resupply settings and post-go-live amendments.
• Participate in quality investigations, CAPA activities, SOP updates, regulatory inspection support, and process improvements.

Requirements

• Associate or bachelor's degree in computer science, life science, business, or a related field.
• 1–3 years of relevant experience in pharma or biotech and cross-functional teams.
• Excellent written and verbal English communication skills required.
• Strong technical, analytical, problem-solving, collaboration, and business partnership skills.
• Ability to work with global teams, partners, and customers in a change-agile environment.
• Availability for meetings with teams in other global time zones outside normal working hours.

Nice to have

• Clinical supply chain, project management, business analysis, or continuous improvement experience.
• Adaptability to changing priorities and requirements.
• Ability to work effectively in a fast-paced environment.

Culture & Benefits

• Hybrid work arrangement in Makati City.
• Structured onboarding and technical training program.
• Collaboration with global clinical supply, technology, study, and vendor teams.
• Opportunity to contribute to quality-focused clinical trial systems and continuous improvement initiatives.
• Equal opportunity employment.