Document Specialist
Summary
Maintains and organizes pharmaceutical research documents, ensuring compliance and completeness of Trial Master Files while handling administrative tasks.
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
- Bachelor's degree;
- Prior administrative experience
- Experience in archiving is a plus
- Full working proficiency in English and Portuguese
- Proficiency in standard MS Office applications
- Detail-oriented mindset and ability to do paperwork
- Good organizational and time-management skills
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.