KCRN Research, Inc. is looking for a qualified candidate for the following position. We are promised to provide better
working environment and you can expand your abilities! If you would like to
become a part of our team, please send your CV to hr@kcrnresearch.com for new
opportunities.
Regulatory Associate, Clinical Operations
[Description] This position is full-time position and primarily
responsible for support electronic regulatory files, including correspondence
for all assigned studies. Regulatory Associate should have strong oral communication
and writing skills. Also, we expect very strong time management skills and
excellent ability to demonstrate client service focus. [Responsibilities]
- Assist
IND preparation works and other regulatory tasks
- Conduct
the assigned works under the guidance of Supervisor
- Support
communicates with the FDA
- Provides
regulatory support and tracks regulatory timelines
- Participate
in a meeting or teleconference with a client
- Update
and report the regulatory project status to Supervisor
- Support
other company operations for relevant matters
[Qualifications]
- Postdoctoral
or equivalent in Life Science or related fields (Preferred)
- Excellent
verbal and written communication skills in English and Korean
- Computer
literate with proficiency of MS Office products and Adobe PDF
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