Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль описана понятно и дает заметную ответственность за проекты и клиентские аккаунты в клинических исследованиях, но план по росту выручки добавляет коммерческую нагрузку к управлению проектами.
План по выручке
Понятные задачи
Клинические исследования
?Удалённо по ЮАР
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Project Manager (CRO - Biometrics) - Home Based (South Africa) (clinical research and biometric deliverables): Managing moderate-complexity clinical research projects covering data management, biostatistics, and statistical programming with an accent on budgets, timelines, financial KPIs, and client relationships. Focus on controlling project scope, resolving risks and issues, coordinating bid activities, and meeting regulatory requirements including ICH, 21 CFR Part 11, and ISO standards.
Location: Remote, based within South Africa; listed locations include Bloemfontein, Johannesburg, Pretoria, Cape Town, Durban, Free State, Gauteng, Western Cape, KZN, North West, and Eastern Cape.
Company
hirify.global is a data-focused clinical research organization supporting pharmaceutical, biotech, and medical device industries with clinical trial data and regulatory submission services.
What you will do
Develop budgets, understand cost models, manage financial KPIs, invoice according to payment schedules, and update revenue projections.
Control project scope through project management and change management processes.
Develop project timelines, use Microsoft Project advanced functions, manage task constraints, and communicate critical path milestones.
Execute day-to-day project activities, identify risks, escalate and resolve issues, and collaborate with functional line management.
Manage at least one key account, strengthen client relationships, develop account growth plans, and target a minimum of 10% annual revenue growth.
Participate in or lead RFIs/RFPs, capabilities meetings, and bid defenses.
Requirements
Bachelor’s degree or relevant work experience.
Minimum 5 years of experience in project coordination, project management, or a similar field.
Expert knowledge of scientific principles and concepts.
Proficiency with Microsoft Office applications, including Word, Outlook, PowerPoint, and intermediate Excel skills such as HLOOKUP, VLOOKUP, and PivotTables.
Good communication, organizational, and collaboration skills, with the ability to understand needs and solve problems.
Excellent problem-solving skills.
Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
Basic understanding of CROs, scientific and clinical data terminology, and the drug development process.
Understanding of general ICH, 21 CFR Part 11, and ISO 9001:2000 requirements.
Nice to have
Hands-on experience with clinical trials and pharmaceutical development.
Familiarity with current ISO 9001 and ISO 27001 standards.
Culture & Benefits
Full-time employment with remote work from within South Africa.
Collaborative and inclusive work environment.
Supportive, innovative organization with a focus on employee retention.
Work with pharmaceutical, biotech, and medical device clients on clinical research projects.
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