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4 дня назад

Site Activation Manager, Sponsor Facing

Формат работы
remote (только Serbia)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Serbia
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
Site Activation Manager, Sponsor Facing (Clinical Research): Leading strategic, operational, and financial delivery of site activation activities across global and multi-regional clinical studies with an accent on site selection, regulatory submissions, contracting, and study start-up. Focus on managing activation plans, navigating regulatory landscapes, mitigating delivery risks, and coordinating sponsors, internal teams, and external stakeholders.

Location: Belgrade, Serbia; homebased

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 clinical studies.
  • Manage study start-up from pre-award through site activation and lifecycle maintenance in line with ICH-GCP, regulatory requirements, and project timelines.
  • Develop and execute Site Activation Management Plans aligned with study strategy and scope of work.
  • Oversee site identification and selection, regulatory submissions, approvals, contracts, essential documents, and project tracking systems.
  • Assess regulatory landscapes, identify risks, and propose solutions supporting study delivery and bid processes.
  • Support business development, client engagement, team mentoring, and continuous improvement initiatives.

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, communication, negotiation, and stakeholder management skills.
  • Ability to deliver projects on time, within scope, and within budget while managing multiple priorities.
  • Expertise in regulatory requirements, clinical trials, quality, and compliance.

Culture & Benefits

  • Homebased work arrangement.
  • Collaboration with internal teams, regional groups, sponsors, clients, and external stakeholders.
  • Opportunities to mentor team members and contribute to continuous improvement.
  • Focus on integrity, quality, compliance, and improving patient outcomes.

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