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 level
- Work closely with site-monitors and interface with site representatives, vendors and PSI project teams
- Be responsible for document management and maintenance of the Trial Master File for your sites and projects
- Update and maintain (automated) tracking systems and schedules
- Coordinate various activities within clinical research projects
- Provide support for administrative tasks, e.g. meeting coordination, agenda and minute preparation on a project level
- College/University degree or an equivalent combination of education, training & experience
- Administrative work experience, preferably in an international setting
- Fluent in English
- MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication and collaboration skills
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.
