Document Management Specialist (Clinical Trial)
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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!
The scope of responsibilities will include:
- Review maintain and archive essential study documents for the Trial Master File
- Communication with multi-functional project teams on document management matters
Qualifications :
- Experience in document management activities is a plus. Fresh graduate are welcome to apply.
- Higher Vocational Certificate (e.g. Marketing General Management or Secretarial Studies).
- Full working proficiency in English and Thai.
- Knowledge of any other language spoken in Asia & Pacific region especially Japanese is a plus.
- Detail-oriented mind-set and organizational skills.
- PC skills to be able to work with MS Word Excel and PowerPoint.
- Communication and collaboration skills.
We encourage junior candidates to apply for this position.
Additional Information :
We offer:
- Excellent flexible working conditions
- Extensive training and supportive team
- Competitive salary and benefits package
Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.
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
