13 дней назад
Senior Site Activation Coordinator (North America)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Site Activation Coordinator (North America): Coordinating feasibility, site activation, and maintenance activities for clinical study sites in accordance with regulations, SOPs, and project requirements with an accent on regulatory documentation, ethics approvals, and site readiness. Focus on reviewing and tracking contractual and regulatory documents, maintaining study systems and timelines, and coordinating completion with site activation and project management teams.
Location: Home-based in São Paulo, Brazil
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform feasibility, site activation, and selected maintenance activities for assigned clinical studies.
- Prepare and review site documents for completeness, consistency, and accuracy.
- Track regulatory, ethics, contractual, informed consent, and investigator pack documents through approval and execution.
- Inform sites and internal project teams when required documentation is complete and distribute finalized documents.
- Maintain study databases, tracking tools, timelines, and project plans with accurate project information.
- Collaborate with the Site Activation Manager, Project Management team, and other departments.
Requirements
- Bachelor’s degree in life sciences or a related field.
- At least 2 years of experience in a contract research organization or more than 4 years of site experience.
- Previous experience with regulatory and site activation activities.
- Advanced English is mandatory for communication with North American sites and global teams.
- Home-based position in São Paulo, Brazil.
Culture & Benefits
- Work from home in a role supporting North American clinical study sites.
- Collaborate with a global team across site activation, project management, and other functions.
- Work within established regulations, standard operating procedures, and project guidelines.
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