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2 часа назад

Global Site Activation Manager, Sponsor Dedicated, Poland

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, Poland (Clinical Research): Leading strategic, operational, and financial site activation activities across global and multi-regional clinical studies with an accent on site selection, regulatory submissions, contracting, and study start-up delivery. Focus on developing activation plans, managing regulatory and contract risks, coordinating cross-functional stakeholders, and delivering projects on time, within scope, and budget.

Location: Homebased in 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.
  • Oversee regulatory submissions, approvals, contracts, essential documents, project systems, timelines, and reporting.
  • Assess regulatory landscapes, identify delivery risks, and contribute to regulatory strategy, bid processes, and bid defense.
  • Build client relationships, support customer-facing activities, and mentor team members.

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.
  • Knowledge of regulatory and clinical trial requirements, including ICH-GCP.

Culture & Benefits

  • Home-based work arrangement.
  • Opportunity to work on global clinical research programs supporting the development of medical treatments.
  • Health and welfare benefits may be provided depending on the position.
  • Potential incentive plans, bonuses, or other compensation may be offered in addition to base pay.

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