Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль четко описана и предполагает серьезную ответственность за онкологические исследования в специализированной CRO-компании, но без указанной зарплаты и с обязательными поездками сложнее оценить условия.
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КомандировкиЗарплата не указанаПонятная зона ответственностиОнкологические исследования
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Project Manager (Oncology): Leading full-service oncology clinical trials for a CRO across global and regional Phase I–IV studies with an accent on operational delivery, client management, budgets, timelines, and quality. Focus on coordinating cross-functional teams, managing study documentation and performance metrics, and delivering complex clinical research programs.
Location: Remote, Poland. Domestic and international travel, including overnight stays, is required.
Company
hirify.global is a people-focused CRO supporting precision medicine, oncology, rare disease research, clinical trial design, biomarker and data analytics solutions.
What you will do
Lead full-service global and regional Phase I–IV oncology clinical trials within agreed scope, budget, timelines, and quality standards.
Manage clinical, medical, safety, data management, biostatistics, and other functional areas throughout the study lifecycle.
Act as the primary client liaison, supporting proposals, client presentations, status reporting, and issue escalation.
Coordinate internal and external project teams and collaborate with senior management and sponsors.
Prepare and review protocols, project plans, informed consents, site contracts, budgets, and other study documentation.
Track deliverables and performance metrics while supporting efficient trial execution.
Requirements
Degree or equivalent qualification in life sciences, or a comparable 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, including experience managing oncology studies and global clinical trials.
Working knowledge of GCP/ICH guidelines, clinical development processes, medical terminology, and clinical trial activities.
Strong communication, presentation, interpersonal, organizational, and relationship-building skills.
Must be legally authorized to work in Poland without employer sponsorship. Effective written and spoken English is required, along with availability for domestic and international travel.
Nice to have
Experience with MS Office, MS Project, PowerPoint, CTMS, eTMF, EDC, and IXRS.
Culture & Benefits
Supportive, collaborative, and high-energy working environment.
Focus on work-life balance and team development.
Opportunity to contribute to research into cancer therapies and precision medicine.
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