Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Это четкая руководящая роль в клинических исследованиях у крупного CRO, но зарплата не указана, а широкий охват задач, высокий темп и поездки затрудняют оценку нагрузки и условий.
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Широкий охватЗарплата не указанаПоездки по работеЧеткая роль лидераКрупный CRO
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
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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