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8 дней назад

Assoc Site Activation Manager - Global Study Leadership

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Argentina/Mexico/Colombia +1 еще
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
Assoc Site Activation Manager - Global Study Leadership (Clinical Research): Leading global study start-up and site activation activities across regional, multi-regional, and global clinical trials with an accent on regulatory submissions, ethics approvals, contracting, and activation strategy. Focus on managing complex timelines, risks, budgets, stakeholder alignment, and critical-path challenges across diverse markets.

Location: Buenos Aires, Argentina; other listed locations: Mexico City, Mexico; São Paulo, Brazil; Bogotá, Colombia

Company

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

What you will do

  • Lead site activation activities from study award through activation across regional, multi-regional, and global clinical trials.
  • Develop and execute Site Activation Management Plans aligned with study strategy, timelines, scope, and customer requirements.
  • Coordinate sponsors, investigative sites, and cross-functional teams on regulatory submissions, ethics approvals, contracting, and country activation.
  • Provide guidance on regulatory requirements, submission strategies, and site activation approaches across global markets.
  • Manage timelines, risks, budgets, scope, quality, and operational performance while resolving critical-path issues.
  • Support proposals and bid defenses, mentor colleagues, and contribute to process improvement and operational excellence.

Requirements

  • Bachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline.
  • 5+ years of experience in site activation, study start-up, regulatory affairs, clinical operations, or a related clinical research environment.
  • Experience leading regional, multi-country, or global site activation activities within a CRO, pharmaceutical, or biotechnology organization.
  • Strong knowledge of clinical trial regulations, ICH-GCP guidelines, ethics submissions, site activation processes, and clinical trial agreements.
  • Experience managing study timelines, risks, quality, budgets, operational performance, and stakeholder relationships.
  • Strong negotiation, communication, leadership, problem-solving, and project management skills.

Culture & Benefits

  • Work with a global, full-service study leadership organization.
  • Support a diverse portfolio including oncology, rare disease, CNS, cardiovascular, immunology, respiratory, cell and gene therapy, infectious disease, ophthalmology, and women’s health.
  • Collaborate with sponsors and global study teams across a worldwide clinical research network.
  • Access mentorship, flexible ways of working, AI-enabled technology, and data-driven insights.
  • Opportunities to broaden clinical research expertise and expand leadership impact.

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