Centralized Monitoring Assistant (Clinical Research)

Location: Home-based in São Paulo, Brazil

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Provide administrative support to clinical study management teams, including system reports, status reports, study trackers, and issue follow-up.
• Maintain project systems and support tracking compliance within study timelines and plans.
• Prepare site and country information packs, process access requests, and support project execution under supervision.
• Review site-level key risk indicators, historical site performance, and the Study Central Monitoring Plan.
• Identify site-level risks and recommend timely corrective actions, such as telephone contacts or triggered onsite monitoring visits.
• Review corrective-action effectiveness, participate in project meetings, and follow statements of work and customer requirements.

Requirements

• Exclusive opportunity for people with disabilities.
• Bachelor’s degree, ideally in Life Sciences.
• 1–2 years of relevant work experience.
• Good command of English is mandatory for collaboration with international teams.
• Ability to complete role-specific training and work in accordance with standard operating procedures, good clinical practices, and regulatory requirements.

Culture & Benefits

• Home-based work arrangement.
• Inclusive work environment committed to diversity and equal opportunity.
• Work supporting the development and commercialization of medical treatments and improved patient outcomes.