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9 часов назад

Central Monitor in LATAM (Clinical Research)

Формат работы
remote (только Brazil)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Brazil
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Central Monitor in LATAM (Clinical Research): Performing centralized monitoring and reviewing structured clinical data and medical charts across clinical research projects, sites, and teams with an accent on study quality, data integrity, and protocol compliance. Focus on managing monitoring triggers, conducting subject-level data reviews, analyzing trends, and escalating site quality issues.

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

  • Perform centralized monitoring activities across assigned clinical research projects, sites, and countries.
  • Evaluate study quality and data integrity against protocols, SOPs, regulations, and guidelines.
  • Manage monitoring triggers and prepare i-site packs for assigned sites and countries.
  • Review structured clinical data and medical charts, including subject-level data requiring further investigation.
  • Support trend analytics, maintain project databases and tracking tools, and participate in cross-functional study meetings.
  • Follow up with sites and CRAs on study milestones, triage data issues, and escalate site quality concerns.

Requirements

  • Bachelor’s degree in life sciences or a related field, nursing qualification, or near-completion of the required degree.
  • At least 2 years of monitoring experience, either onsite or remote.
  • Advanced Excel skills.
  • Advanced English is mandatory for supporting sites in Latin America or North America.
  • Clinical experience and the ability to review patient information, medical charts, and study data for accuracy.

Culture & Benefits

  • Home-based remote work arrangement.
  • Work across multiple clinical research projects, sites, and cross-functional teams.
  • Opportunity to contribute to the development and commercialization of medical treatments and improved patient outcomes.

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