Document Specialist
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Job Location:
Monthly Salary:
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Department:
Job Summary
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
Qualifications :
- Bachelors 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
Additional Information :
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 well be there with you every step of the way.
Remote Work :
No
Employment Type :
Full-time
Key Skills
- DRG
- Acute Care
- Adobe Acrobat
- ICD-10
- Records Management
- Technical Writing
- Clinical Documentation Improvement
- Documentation Review
- Sharepoint
- cGMP
- Document Management Systems
- Document Management
About Company
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on on-time project delivery. This is achieved through investing substantial effo ... View more
