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7 часов назад

Clinical Research Associate, Single Sponsor Dedicated in Poland

119 400 - 280 000PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
junior
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
Clinical Research Associate, Single Sponsor Dedicated in Poland (Clinical Trials): Monitoring and managing clinical trial sites in line with study protocols, regulations, GCP/ICH guidelines, and sponsor requirements with an accent on site selection, initiation, monitoring, close-out, and documentation. Focus on tracking recruitment, regulatory submissions, CRF completion, data query resolution, and escalating quality issues.

Location: Warsaw, Poland; remote role with on-site clinical trial monitoring visits

Salary: 119,400–280,000 PLN annualized

Company

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

What you will do

  • Perform site selection, initiation, monitoring, and close-out visits.
  • Maintain appropriate clinical trial documentation and ensure protocol compliance.
  • Support subject recruitment planning and track recruitment progress.
  • Establish communication with assigned sites and deliver protocol and study-related training.
  • Evaluate site practice quality and integrity, escalating issues when necessary.
  • Track regulatory submissions, CRF completion, and data query resolution.

Requirements

  • Bachelor’s degree in a scientific discipline or healthcare.
  • At least one year of experience in on-site clinical trial monitoring.
  • Knowledge of clinical research regulations, including GCP and ICH guidelines.
  • Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices.
  • Good command of Polish and English is required.
  • Ability to build and maintain effective relationships with colleagues, managers, and clients.

Culture & Benefits

  • Full-time employment with potential incentive plans, bonuses, and additional compensation.
  • Health, welfare, and other benefits may be provided.
  • Commitment to diversity, inclusion, and a respectful workplace.
  • Work focused on supporting the development of medical treatments and improving patient outcomes.

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