Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чёткая зона ответственности за международные онкологические исследования и специализация в здравоохранении делают вакансию привлекательной, но зарплата не указана, а командировки обязательны.
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КомандировкиЗарплата не указанаПонятная зона ответственностиОнкологические исследованияБаланс работы и жизни
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Project Manager (Oncology): Leading full-service global and regional oncology clinical trials from proposal strategy through completion with an accent on operational delivery, cross-functional oversight, client relationships, budgets, timelines, and quality. Focus on coordinating functional teams, managing complex study documentation and performance metrics, and delivering clinical development programs in compliance with GCP/ICH guidelines.
Location: Remote, Hungary. Domestic and international travel, including overnight stays, is required. Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Company
hirify.global is a people-focused contract research organization combining clinical trial operations, medical expertise, precision medicine, biomarker solutions, and data analytics for oncology and rare disease programs.
What you will do
Lead full-service global and regional Phase I–IV oncology clinical trials from proposal strategy and bid defense through study completion.
Own project delivery against scope, budget, timelines, quality requirements, and financial objectives.
Coordinate functional areas including data management, safety, clinical operations, medical monitoring, and biostatistics.
Act as the primary client liaison and participate in proposals, client presentations, and senior stakeholder meetings.
Manage project teams, sponsors, deliverables, performance metrics, escalations, and status reporting.
Prepare and review protocols, project plans, informed consents, site contracts, budgets, and other study documentation.
Requirements
Degree or equivalent qualification in life sciences, or an equivalent combination of education and experience.
At least 4 years of full-service clinical project management experience in a CRO or clinical research organization.
Extensive clinical operations experience in a CRO and experience managing oncology studies.
Working knowledge of GCP/ICH guidelines, clinical development processes, medical terminology, and clinical trial activities.
Effective written and spoken English communication, strong presentation skills, and proven ability to build positive internal and external working relationships.
Experience with MS Office, MS Project, PowerPoint, CTMS, eTMF, EDC, and IXRS.
Culture & Benefits
Supportive, collaborative environment within a people-focused CRO.
Work-life balance and encouragement for team development.
Opportunity to contribute to clinical programs advancing oncology and precision medicine.
Exposure to international clinical trials and cross-functional global collaboration.
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