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Global Site Activation Manager (Clinical Research)

Формат работы
remote (только South_africa)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
SA
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 strategic, operational, and financial delivery of site activation activities across global and multi-regional clinical studies with an accent on regulatory submissions, site contracting, study start-up, and lifecycle maintenance. Focus on developing activation strategies, managing cross-functional delivery and risks, supporting client and bid activities, and mentoring teams.

Location: Homebased in Centurion, South Africa

Company

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

What you will do

  • Lead strategic, operational, and financial delivery of site activation activities across global and multi-regional studies.
  • Manage study start-up from pre-award through activation, including site identification, selection, regulatory submissions, ethics approvals, contracting, and lifecycle maintenance.
  • Develop and execute Site Activation Management Plans aligned with study strategy and scope of work.
  • Coordinate internal teams, regional stakeholders, sponsors, and external partners to deliver studies on time and within scope and budget.
  • Assess regulatory landscapes, manage risks, maintain project systems and documentation, and contribute to regulatory strategy.
  • Support business development, client engagement, bid defense, team mentoring, and continuous improvement.

Requirements

  • Bachelor’s degree in Life Sciences or a related field.
  • At least 7 years of clinical research experience, including 3 or more years in a leadership role.
  • International project experience across multiple regions.
  • Strong leadership, project management, strategic thinking, and problem-solving skills.
  • Experience delivering projects on time, within scope, and budget while managing multiple priorities.
  • Strong communication, negotiation, stakeholder management, regulatory, clinical trial, quality, and compliance expertise.

Culture & Benefits

  • Homebased work arrangement.
  • Cross-functional collaboration across global and regional teams.
  • Opportunities to mentor team members and contribute to continuous improvement.
  • Work focused on accelerating clinical study activation and the development of medical treatments.

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