Company Description
PSI is a leading Contract Research Organization with more than 29 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.
We focus on delivering quality and on-time services across a variety of therapeutic indications.
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems, and managing documents & information.
Office Based in Madrid
You will: Assist project teams with selective aspects of trial management from start-up to close-out on a country levelWork closely with site-monitors and interface with site representatives, vendors, and PSI project teamsBe responsible for document management and maintenance of the Trial Master File for your sites and projectsUpdate and maintain (automated) tracking systems and schedulesCoordinate various activities within clinical research projectsProvide support for administrative tasks, e.g., meeting coordination, agenda, and minute preparation on a project level Qualifications College/University degree or an equivalent combination of education, training & experienceAdministrative work experience, preferably in an international settingFluent in EnglishAbility to plan, multitask and work in a dynamic team environmentCommunication and collaboration skills Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
PSI is an inclusive and equal opportunity employer and is committed to attracting and retaining a diverse workforce that reflects the community we serve.
Applications from Aboriginal and Torres Strait Islanders are encouraged.
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