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2 часа назад

Global Site Activation Manager, Sponsor Dedicated, Slovakia

201 500 - 374 100PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Poland
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, Sponsor Dedicated, Slovakia (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 lifecycle maintenance. Focus on accelerating study start-up, managing regulatory and delivery risks, coordinating cross-functional stakeholders, and maintaining compliance with ICH-GCP and project requirements.

Location: Homebased, Warsaw, Poland

Salary: zł201,500–zł374,100 annualized base pay

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 activation, including site identification, selection, regulatory submissions, ethics approvals, and site contracting.
  • 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 support timely study delivery.
  • Assess regulatory landscapes, manage risks, and contribute to regulatory intelligence, bid defense, and client engagement.
  • Maintain accurate project tracking, reporting, documentation, and continuous improvement activities while mentoring team members.

Requirements

  • Bachelor’s degree in Life Sciences or a related field.
  • At least 7 years of clinical research experience, including 3+ years in a leadership role.
  • International project experience across multiple regions.
  • Strong project management, leadership, communication, negotiation, and stakeholder management skills.
  • Experience delivering projects on time, within scope, and within budget.
  • Knowledge of regulatory and clinical trial requirements, including ICH-GCP compliance.

Culture & Benefits

  • Homebased work arrangement.
  • Health and welfare benefits may be provided depending on the position.
  • Potential incentive plans, bonuses, and other forms of compensation may be available.
  • Opportunities to contribute to team development and continuous improvement.

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