Assoc Site Activation Manager - Global Study Leadership
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Argentina/Mexico/Colombia +1 еще
aiproject managementregulatory affairsclinical researchclinical operationsich gcpsite activationstudy start up
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Assoc Site Activation Manager - Global Study Leadership (Clinical Research): Leading global study start-up and site activation activities across regional, multi-regional, and global clinical trials with an accent on regulatory submissions, ethics approvals, contracting, and activation strategy. Focus on managing complex timelines, risks, budgets, stakeholder alignment, and critical-path challenges across diverse markets.
Location: Buenos Aires, Argentina; other listed locations: Mexico City, Mexico; São Paulo, Brazil; Bogotá, Colombia
Company
hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
Lead site activation activities from study award through activation across regional, multi-regional, and global clinical trials.
Develop and execute Site Activation Management Plans aligned with study strategy, timelines, scope, and customer requirements.
Coordinate sponsors, investigative sites, and cross-functional teams on regulatory submissions, ethics approvals, contracting, and country activation.
Provide guidance on regulatory requirements, submission strategies, and site activation approaches across global markets.
Manage timelines, risks, budgets, scope, quality, and operational performance while resolving critical-path issues.
Support proposals and bid defenses, mentor colleagues, and contribute to process improvement and operational excellence.
Requirements
Bachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline.
5+ years of experience in site activation, study start-up, regulatory affairs, clinical operations, or a related clinical research environment.
Experience leading regional, multi-country, or global site activation activities within a CRO, pharmaceutical, or biotechnology organization.
Strong knowledge of clinical trial regulations, ICH-GCP guidelines, ethics submissions, site activation processes, and clinical trial agreements.
Experience managing study timelines, risks, quality, budgets, operational performance, and stakeholder relationships.
Strong negotiation, communication, leadership, problem-solving, and project management skills.
Culture & Benefits
Work with a global, full-service study leadership organization.
Support a diverse portfolio including oncology, rare disease, CNS, cardiovascular, immunology, respiratory, cell and gene therapy, infectious disease, ophthalmology, and women’s health.
Collaborate with sponsors and global study teams across a worldwide clinical research network.
Access mentorship, flexible ways of working, AI-enabled technology, and data-driven insights.
Opportunities to broaden clinical research expertise and expand leadership impact.
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