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2 дня назад

Project Support Specialist (Clinical Research)

97 600 - 146 400PLN
Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
middle
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
Project Support Specialist (Clinical Research): Supporting clinical study teams by maintaining project timelines, trial management systems, training records, study documentation, supplies, and communications with an accent on cross-functional coordination, regulatory documentation, and operational accuracy. Focus on managing study systems and access, coordinating materials and reports, and supporting efficient execution across clinical trial phases.

Location: Fully home-based in Poland, Serbia, Slovakia, Hungary, or Romania

Salary: 97,600–146,400 PLN gross per annum in Poland; eligible for a discretionary annual bonus.

Company

hirify.global is a Clinical Research Organization supporting precision medicine, oncology, rare disease, biomarker, data analytics, and targeted clinical trial development.

What you will do

  • Create and maintain project timelines, study trackers, milestone dates, and operational updates.
  • Schedule meetings, prepare agendas, record and distribute minutes, and file documentation in the Trial Master File.
  • Maintain Clinical Trial Management System records, study contacts, enrolment projections, user access, and helpdesk requests.
  • Coordinate study-specific training, training records, shared workspaces, project mailboxes, study supplies, binders, and other study materials.
  • Prepare and distribute communications, safety reports, newsletters, site information, and study updates as directed by project leadership.
  • Act as a point of contact for project-related requests and support clinical trial reports, translations, and material reconciliation.

Requirements

  • Four-year college degree or equivalent experience, ideally in business, science, or healthcare.
  • At least two years of relevant experience as a Clinical Trial Assistant, Clinical Support Specialist, or in a similar role.
  • Fluency in Microsoft Office, including Outlook, Word, Excel, and PowerPoint.
  • Professional-level English proficiency is required.
  • Working knowledge of ICH-GCP, Precision standard operating procedures, and regulatory guidance.
  • Strong communication, interpersonal, organizational, problem-solving, teamwork, and independent planning skills, with close attention to detail.

Culture & Benefits

  • Fully home-based work within the listed Central and Eastern European countries.
  • Private medical insurance and life insurance.
  • MultiSport Card and pension benefits.
  • Home working allowance and vacation benefits.
  • Eligibility for a discretionary annual bonus.

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