Site Management Associate I.

hace 2 semanas


Buenos Aires, Argentina PSI A tiempo completo

Job Description

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. 

Only CVs in English will be accepted.

You will be responsible for:

Maintenance of databases and tracking systems Work with large amount of documents, including their 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, project training and access to vendor-related systems for site teams Receiving and routing all mails and incoming calls Assistance with meeting arrangements Preparation of draft agendas and minutes of project meetings

Qualifications

College/University Degree in Life Sciences;  Administrative work experience, preferably in an international settings; Prior experience working as CTA for CROs; Prior experience working in Clinical Research;  Local regulations knowledge; Full working proficiency in English and Spanish; Proficiency in MS Office applications; Ability to plan and work in a dynamic team environment; Communication and collaboration skills.

Additional Information

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.



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