Global Site Activation Manager (Clinical Research)
Контакты
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Serbia/Spain/Latvia +3 еще
project managementstakeholder managementregulatory affairsclinical researchclinical trialsich gcpsite activationstudy start up
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
ЗП не указана
На похожих ролях по рынку
$44к$60кмедиана$79к
50 в выборке
На СНГ рынке: $2.2к/мес ($1.5к - $3к)
76
Хорошая вакансия
развернуть
Чёткие глобальные обязанности, развитие карьеры и работа в клинических исследованиях делают вакансию привлекательной, но без зарплаты сложнее оценить условия оплаты.
Кликните для подробной информации
Зарплата не указанаПонятные задачиРазвитие карьерыВклад в медицину
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Global Site Activation Manager (Clinical Research): Leading site activation and study start-up activities for global clinical trials with an accent on regulatory submissions, ethics approvals, contracting, and cross-functional coordination. Focus on managing complex timelines, risks, budgets, compliance requirements, and stakeholder relationships across countries and regulatory environments.
Location: Centurion, South Africa; other listed locations: Belgrade, Serbia; Tartu, Estonia; Sofia, Bulgaria; Riga, Latvia; Madrid, Spain.
Company
hirify.global provides clinical research services, commercial insights, and healthcare intelligence for life sciences and healthcare organizations.
What you will do
Lead site activation and study start-up activities across global, regional, and country-level clinical trial programs.
Manage site identification, feasibility, regulatory submissions, ethics approvals, site contracting, and protocol amendments.
Develop and execute Site Activation Management Plans aligned with study strategy and objectives.
Drive start-up timelines, milestones, budgets, risks, metrics, and performance indicators.
Partner with sponsors, sites, and cross-functional stakeholders to resolve issues and support successful trial delivery.
Prepare updates, reports, presentations, proposal materials, and customer engagement content while mentoring colleagues.
Requirements
Bachelor's degree in Life Sciences or a related field.
Experience in site activation, study start-up, protocol amendments, regulatory affairs, or clinical operations.
Strong knowledge of ICH-GCP, clinical trial regulations, ethics processes, and regulatory requirements.
Experience managing timelines, budgets, risks, and cross-functional stakeholders.
Strong communication, negotiation, planning, organizational, and problem-solving skills.
Ability to lead complex projects and work across cultures and geographies.
Culture & Benefits
Global Study Leadership work across diverse therapeutic areas, countries, regulatory environments, and delivery models.
Structured career development, tailored training, mentorship, and opportunities to move across Site Activation, Clinical, Project Management, and Oversight roles.
Collaborative and flexible working environment supported by AI-enabled technologies.
Opportunity to contribute to clinical research and accelerate the delivery of new treatments to patients.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →