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2 дня назад

Clinical Trial Manager (Oncology)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Serbia/Poland/Romania +2 еще
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 Trial Manager (Oncology) (clinical trials/oncology): Managing and delivering clinical trial operations across multiple countries with an accent on site selection, start-up, enrolment, monitoring, data cleaning, regulatory documentation, and close-out. Focus on leading CRAs, identifying timeline risks, coordinating cross-functional teams, and ensuring quality execution of oncology studies.

Location: Remote in Hungary, Poland, Romania, Serbia or Slovakia. Domestic and international travel, including overnight stays, is required.

Company

hirify.global is a precision medicine CRO delivering oncology and rare disease clinical trials through integrated clinical operations, biomarker science, data analytics, and specialized expertise.

What you will do

  • Manage and deliver clinical trial activities including site selection, study start-up, enrolment, site engagement, monitoring, data cleaning, and close-out.
  • Lead CRAs and oversee monitoring, regulatory, investigational product, site payment, and site correspondence activities.
  • Ensure trial deliverables, timelines, quality standards, regulatory documentation, and operational oversight across multiple countries.
  • Identify risks and challenges affecting study timelines and develop action plans with the team and sponsor.
  • Mentor and train team members while maintaining effective cross-functional communication and client satisfaction.

Requirements

  • Bachelor’s degree or equivalent education and experience in a science or health-related field.
  • Significant clinical trial management and oncology experience, including clinical leadership across multiple countries in a CRO, pharmaceutical, or biotech organization.
  • Working knowledge of GCP, ICH guidelines, regulatory guidance, and the clinical development process.
  • Effective English communication is required.
  • Experience with MS Office, MS Project, PowerPoint, CTMS, eTMF, EDC, and IXRS.
  • Ability to build positive relationships, understand medical terminology, manage shifting priorities, and work autonomously.

Culture & Benefits

  • Remote work from one of five eligible European countries.
  • Autonomy, ownership, and responsibility for clinical trial outcomes.
  • Dynamic work focused on precision medicine, oncology, biomarkers, advanced data platforms, and adaptive clinical trials.
  • Opportunities to mentor team members and collaborate with sponsors and cross-functional teams.
  • Employment requires legal authorization to work in the country of employment without employer sponsorship.

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