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6 дней назад

Project Director (Oncology)

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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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Project Director (Oncology/Clinical Trials): Overseeing global and complex oncology clinical trials or portfolios, including client liaison, project planning, budgets, quality management, and cross-functional execution with an accent on strategic planning, risk mitigation, financial control, and ICH-GCP compliance. Focus on leading project managers and study teams, managing trial performance and profitability, resolving protocol and quality issues, and supporting bid defense and continuous process improvement.

Location: Fully remote from the United Kingdom, Spain, Poland, Hungary, Romania, Serbia or Slovakia. International and domestic travel, including overnight stays, may be required.

Company

hirify.global is a people-focused contract research organization combining clinical trial design, operational and medical expertise, biomarker and data analytics solutions, and oncology and rare-disease research.

What you will do

  • Serve as the primary client liaison and support proposals, client presentations, and bid defense activities.
  • Oversee complex oncology clinical trials or portfolios from establishment and planning through execution and closeout.
  • Direct project managers and cross-functional study teams, setting expectations and driving delivery against project goals.
  • Manage study budgets, profitability, billable hours, forecasting, scope changes, and change orders.
  • Develop project plans, timelines, risk mitigation strategies, quality processes, metrics, and status reporting.
  • Lead meetings, resolve study and protocol issues, ensure training compliance, mentor project managers, and support continuous 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 and at least 5 years of direct project management experience.
  • Experience managing highly complex global studies or portfolios, preferably in pharmaceutical and/or device research.
  • Proficiency with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, and project management software.
  • Mastery of ICH-GCP, project planning, risk management, change management, cross-functional leadership, and quality management.
  • Excellent communication, presentation, negotiation, analytical, organizational, and interpersonal skills.

Culture & Benefits

  • Fully remote work from specified European countries.
  • Supportive and collaborative environment focused on work-life balance.
  • Opportunities for team development, mentoring, and contribution to company SOPs.
  • Work on clinical research supporting innovative cancer therapies and precision medicine.

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