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10 дней назад

Global Site Activation Manager (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Serbia/Spain/Latvia +3 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
Global Site Activation Manager (Clinical Research): Leading site activation and study start-up activities for global clinical trials with an accent on regulatory submissions, ethics approvals, contracting, and cross-functional coordination. Focus on managing complex timelines, risks, budgets, compliance requirements, and stakeholder relationships across countries and regulatory environments.

Location: Centurion, South Africa; other listed locations: Belgrade, Serbia; Tartu, Estonia; Sofia, Bulgaria; Riga, Latvia; Madrid, Spain.

Company

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

What you will do

  • Lead site activation and study start-up activities across global, regional, and country-level clinical trial programs.
  • Manage site identification, feasibility, regulatory submissions, ethics approvals, site contracting, and protocol amendments.
  • Develop and execute Site Activation Management Plans aligned with study strategy and objectives.
  • Drive start-up timelines, milestones, budgets, risks, metrics, and performance indicators.
  • Partner with sponsors, sites, and cross-functional stakeholders to resolve issues and support successful trial delivery.
  • Prepare updates, reports, presentations, proposal materials, and customer engagement content while mentoring colleagues.

Requirements

  • Bachelor's degree in Life Sciences or a related field.
  • Experience in site activation, study start-up, protocol amendments, regulatory affairs, or clinical operations.
  • Strong knowledge of ICH-GCP, clinical trial regulations, ethics processes, and regulatory requirements.
  • Experience managing timelines, budgets, risks, and cross-functional stakeholders.
  • Strong communication, negotiation, planning, organizational, and problem-solving skills.
  • Ability to lead complex projects and work across cultures and geographies.

Culture & Benefits

  • Global Study Leadership work across diverse therapeutic areas, countries, regulatory environments, and delivery models.
  • Structured career development, tailored training, mentorship, and opportunities to move across Site Activation, Clinical, Project Management, and Oversight roles.
  • Collaborative and flexible working environment supported by AI-enabled technologies.
  • Opportunity to contribute to clinical research and accelerate the delivery of new treatments to patients.

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