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15 часов назад

Associate Director Senior Study Lead (Clinical Research)

217 800 - 521 000PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
director
Английский
c1
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
Associate Director Senior Study Lead (Clinical Research): Leading cross-functional clinical trial teams and managing global clinical studies end-to-end with an accent on operational planning, risk management, study delivery, and budget oversight. Focus on guiding complex Phase I–IV studies, coordinating virtual teams in a matrix environment, and ensuring compliance with GCP/ICH and health authority requirements.

Location: Home-based in Warsaw, Poland; only candidates based in the listed location will be considered.

Annual base pay range: 217,800–521,000 PLN.

Company

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

What you will do

  • Lead cross-functional clinical trial teams and guide study-level planning and decision-making.
  • Manage assigned clinical studies from planning through execution, reporting, and delivery.
  • Act as the clinical trial team product owner within agile ways of working.
  • Oversee study budgets, resource allocation, patient recruitment, documentation, and reports.
  • Promote operational excellence through protocol, clinical study report, and study-document development.
  • Drive proactive contingency planning, risk management, stakeholder alignment, and process improvement.

Requirements

  • Bachelor’s degree in life sciences, healthcare, or a clinically relevant field; an advanced degree is strongly preferred.
  • At least 4 years of recent clinical research or drug development experience across Phase I–IV studies.
  • At least 3 years of experience conducting standard-to-high-complexity clinical studies in a pharmaceutical company or contract research organization.
  • Expert knowledge of international standards, including GCP and ICH, and experience with FDA, EMA, and local or national health authorities.
  • Experience leading virtual teams, managing people globally, and building relationships with internal and external stakeholders.
  • Fluent English, oral and written, is required.

Culture & Benefits

  • Home-based working arrangement.
  • Work within a global, matrixed clinical operations environment.
  • Health and welfare benefits may be provided.
  • Incentive plans, bonuses, or other compensation may be available depending on the position.

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