Site Management Associate I.

Job DescriptionJoin 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 meetingsQualifications- 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 InformationAdvance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.