If you are keen to provide administrative, document management support to pharmaceutical research projects, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!
Only CVs in English will be considered.
Responsibilities for this role include:
- Maintaining PSI and client Trial Master File (TMF), as applicable
- Archiving document hard copies in a standardized way
- Reviewing and reporting TMF completeness to project teams, as applicable
- Ensuring compliance with applicable procedures and policies
Requirements
- Bachelor's degree;
- Prior administrative experience
- Experience in archiving is a plus
- Full working proficiency in English and Spanish; Portuguese is a plus
- Proficiency in standard MS Office applications
- Detail-oriented mindset and ability to do paperwork
- Good organizational and time-management skills
PSI CRO
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees
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