Remote Clinical Admin & Site Coordination Associate

Psi CRO; Noord-Holland; Teletrabalho; EUR 30 000 - 42 000; Tempo integral

Resumo da oferta

Psi CRO is seeking an administrative/documentation specialist to support clinical research operations from a remote Netherlands base. You will manage databases, handle documents, translate and file materials, and coordinate with internal teams and external sites.

You have at least 6 months of clinical research administrative experience, a Life Sciences degree, and professional Dutch and English proficiency, with strong organizational and multitasking abilities.

Qualificações

• At least 6 months of experience in administrative and documentation management within clinical research.
• Life Sciences university degree.
• Full professional working proficiency in Dutch and English.
• Good organizational and planning skills.
• Detail-oriented and able to multi-task in a fast-paced environment.
• Proficiency in MS Office applications (Word, Excel and PowerPoint).

Responsabilidades

• Maintenance of databases and tracking systems.
• Work with large amounts of documents, including compiling, procurement, processing, translation and filing.
• Communication with company departments and external parties.
• Communication point for investigative sites participating in the clinical research projects.
• Coordination of site-specific query resolution and project training; access to vendor systems for site teams.
• Receiving and routing all mails and incoming calls.
• Assistance with meeting arrangements; preparation of agendas and minutes of project meetings.

Conhecimentos

Dutch proficiency

English proficiency

Organizational skills

Multi-tasking

Customer service

Formação académica

Life Sciences degree

Ferramentas

MS Office (Word, Excel, PowerPoint)

Descrição da oferta de emprego

Psi CRO is seeking an administrative/documentation specialist to support clinical research operations from a remote Netherlands base. You will manage databases, handle documents, translate and file materials, and coordinate with internal teams and external sites.

You have at least 6 months of clinical research administrative experience, a Life Sciences degree, and professional Dutch and English proficiency, with strong organizational and multitasking abilities.