Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль описана понятно и предполагает руководство значимыми онкологическими исследованиями, но зарплата не указана, а международные поездки могут повлиять на образ жизни.
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КомандировкиЗарплата не указанаПонятная зона ответственностиОнкологические исследованияБаланс и развитие
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Project Manager (Oncology) (Clinical Trials/CRO): Leading full-service phase I–IV oncology clinical trials from proposal strategy and costing through completion with an accent on project delivery, functional oversight, client relationships, budgets, timelines, and quality. Focus on coordinating cross-functional teams, managing global and regional studies, reviewing clinical documentation, and resolving complex operational challenges across clinical development programs.
Location: Remote, United Kingdom. Domestic and international travel, including overnight stays, is required.
Company
hirify.global is a people-focused CRO delivering clinical trials, precision medicine solutions, biomarker and data analytics services, and medical expertise for oncology and rare disease programs.
What you will do
Lead full-service phase I–IV clinical projects in oncology according to the agreed scope, budget, timelines, and quality standards.
Manage all study stages, from proposal strategy, costing, and bid defense through study completion.
Oversee cross-functional teams covering clinical operations, data management, safety, medical monitoring, biostatistics, and other functions.
Act as the primary client liaison, participate in presentations, and maintain relationships with sponsors and senior management.
Prepare project plans, status reports, performance metrics, protocols, informed consent documents, site contracts, and budgets.
Coordinate internal and external stakeholders, identify risks and escalations, and drive 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 within a CRO, with extensive clinical operations experience.
Experience managing oncology studies and global or regional clinical trials.
Working knowledge of GCP/ICH guidelines, clinical development processes, medical terminology, and clinical trial activities.
Strong written and spoken English, presentation, interpersonal, organizational, and relationship-building skills.
Experience with MS Office, MS Project, PowerPoint, CTMS, eTMF, EDC, and IXRS.
Culture & Benefits
Remote work arrangement for the United Kingdom.
Supportive, collaborative, and high-energy working environment.
Focus on work-life balance and team development.
Opportunity to contribute to clinical programs developing cancer therapies.
Must be legally authorized to work in the United Kingdom without employer sponsorship.
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