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8 дней назад

Trial Clinical Delivery Lead

Формат работы
remote (только Europe)/onsite
Тип работы
fulltime
Грейд
senior/lead
Английский
c1
Страна
UK/Poland/Spain +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
Trial Clinical Delivery Lead (Clinical Research): Leading delivery and quality oversight for Phase I–IV clinical, epidemiology, real-world evidence, and early access studies with an accent on risk-based site oversight, operational planning, and cross-functional leadership. Focus on interpreting study performance data, designing monitoring and country start-up strategies, resolving delivery risks, and coordinating clinical operations across sponsors, CROs, and global functions.

Location: Prague, Frankfurt, Dublin, Warsaw, Lisbon, Madrid, or Reading; remote or office-based. Domestic or international travel may be required for up to 20% of the time.

Company

hirify.global Strategic Solutions provides sponsor-dedicated functional service provision and clinical research services for multinational pharmaceutical partners.

What you will do

  • Lead delivery and quality oversight for Phase I–IV clinical development, epidemiology, real-world evidence, company-sponsored, collaborative, investigator-sponsored, and early access studies.
  • Provide strategic and operational leadership for Clinical Site Leads and Clinical Research Managers across assigned programs and studies.
  • Use site performance, quality, and analytical data to drive risk-based oversight, monitoring strategies, site selection, and study execution.
  • Develop country start-up strategies and Site Oversight Plans in collaboration with clinical trial, CRO, and country start-up functions.
  • Identify trends, risks, quality issues, timeline or cost impacts, and coordinate mitigation and escalation plans.
  • Represent clinical operations in governance, launch, brand, medical affairs, and cross-functional study meetings.

Requirements

  • Graduate degree in medical or life sciences, clinical research, or an equivalent discipline.
  • At least 10 years of professional and project management experience in clinical research within a CRO, pharmaceutical, or biotech company.
  • Strong clinical operations experience across Phase I–IV studies, including site management, oversight, study planning, and conduct.
  • Expert knowledge of clinical development principles, ICH GCP, and applicable regional and local regulations.
  • Fluent English and the relevant local language required.
  • Ability to assess risk, solve problems, make decisions, manage multiple priorities, and communicate effectively with internal and external partners.

Nice to have

  • Experience in oncology, neurology, or immunology therapeutic areas.
  • Experience interpreting analytical tools and applying data-driven approaches to study execution.

Culture & Benefits

  • Sponsor-dedicated work supported by hirify.global’s global clinical research expertise.
  • Collaborative environment with opportunities for career development and operational leadership.
  • Country-specific annual leave, health insurance, retirement planning, life assurance, and optional benefits.
  • Global Employee Assistance Programme and workplace inclusion and accessibility support.

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