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7 часов назад

Clinical Operations Manager Cluster South

Формат работы
remote (только Argentina)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US/Argentina
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Clinical Operations Manager Cluster South (Clinical Research): Managing site-related clinical study execution across start-up, execution, and close-out phases with an accent on site oversight, regulatory compliance, and resource planning. Focus on ensuring audit readiness, coordinating monitoring activities, developing clinical operations talent, and delivering studies on time and within budget.

Location: Buenos Aires, Argentina

Company

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

What you will do

  • Lead site-related clinical study execution through start-up, conduct, and close-out, including country and site feasibility.
  • Oversee site selection, contract and budget negotiations, regulatory and ethics committee submissions, monitoring, issue management, and site closure.
  • Ensure compliance with applicable regulations, Good Clinical Practice, ICH guidelines, standard operating procedures, monitoring plans, and quality standards.
  • Maintain audit and inspection readiness, including pre-audit activities, site and system audits, and CAPA follow-up.
  • Manage study resources and support hiring, onboarding, performance management, mentoring, and development of clinical operations staff.
  • Coordinate with CROs and global or local stakeholders on complex studies, training initiatives, and remote data review activities when assigned.

Requirements

  • Bachelor’s degree or equivalent in a health-related field such as medicine, science, nursing, or pharmacy.
  • At least 3 years of clinical monitoring experience.
  • Experience across multiple therapeutic areas and study phases.
  • Strong planning, organizational, interpersonal, communication, mentoring, and coaching skills.
  • Ability to work independently, manage ambiguity, make timely decisions, and adapt to changing requirements.
  • Commitment to integrity, continuous improvement, collaboration, and high-quality clinical research execution.

Culture & Benefits

  • Work within a global research organization focused on improving patient lives.
  • Emphasis on innovation, integrity, collaboration, and continuous process improvement.
  • Equal opportunity employment environment.

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