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2 дня назад

Project Director (Clinical Trials)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
UK/Serbia/Poland +4 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 Director (Clinical Trials): Leading complex global clinical trials and portfolios in oncology, with an accent on client liaison, study execution, financial oversight, quality management, and cross-functional leadership. Focus on developing strategic project plans, managing risks and change, maintaining inspection readiness, and driving trial performance across international teams.

Location: Fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia

Company

hirify.global is a clinical research organization supporting precision medicine, rare disease, and oncology studies through clinical trial design, operational expertise, medical oversight, biomarker solutions, and data analytics.

What you will do

  • Serve as the primary client liaison and participate in proposals, client presentations, and bid defense activities.
  • Oversee complex clinical trials, global studies, or portfolios of studies from planning and initiation through execution and closeout.
  • Direct project managers and cross-functional teams while coordinating study strategies, timelines, training, and delivery.
  • Manage study budgets, profitability, billable hours, forecasting, scope, change orders, and financial performance.
  • Lead risk management, change management, quality management, inspection readiness, issue escalation, and corrective actions.
  • Prepare status updates and performance metrics for clients and senior management, mentor project staff, and support continuous process improvement.

Requirements

  • Degree or equivalent education and experience in a science or health-related field; an advanced degree is preferred.
  • At least 8 years of clinical research experience, including a minimum of 5 years of direct project management experience.
  • Experience managing highly complex global studies or a portfolio of studies in pharmaceutical and/or device research.
  • Strong knowledge of ICH-GCP, SOPs, project management techniques, strategic planning, risk management, and change management.
  • Proficiency with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, and project management software.
  • Excellent communication, presentation, negotiation, organizational, analytical, leadership, and customer management skills.

Culture & Benefits

  • Fully remote work from the listed European countries.
  • Supportive and collaborative environment focused on work-life balance and team development.
  • Opportunity to contribute to clinical research for innovative cancer therapies and precision medicine.
  • Domestic and international travel, including overnight stays, may be required.

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