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发帖数: 12 | 1 A world leading pharmaceutical company is currently recruiting a Regulatory
Medical Writer based in Beijing, China (JD as below). Fresh Biology Ph.D is
welcomed if you want to explore opportunities other than doing bench work.
If you are interested, CV can be sent to [email protected]
POSITION SUMMARY
As an integral part of the clinical team, medical writer in the ×× group
of China R&D center ensures the quality, compliance with internal and
external standards, and timely production of both English and Chinese-
language clinical documents, according to company guidelines and
international regulations.
KEY ACCOUNTABILITIES
1. Writing, summarizing, editing, and reviewing documents, or sections
of
documents (eg, protocol, clinical study report, summary documents)
2. Ensuring architecture and content that concisely and effectively
transmit strategic information
3. Coordinating the activities within the group, and those with
interfaces in Platform, other Units, or external collaborators, to ensure
timely completion of deliverables
4. Defining and proposing best timelines for the group deliverables, in
collaboration with authoring or submission teams
5. Defining and requesting quality control for the group deliverables
JOB-HOLDER ENTRY REQUIREMENTS
Education & Experience:
A candidate with a scientific degree, preferably PhD, majoring in medicine,
pharmacy, or life science related disciplines.
A 2-4 years’ experience in pharmaceutical industry or publications in the
international journals as the first author would be an asset.
Core competencies:
Good command of both English and Chinese (written and verbal)
Ability to communicate clinical data succinctly, clearly and accurately in
writing
Proactive, accountable, details oriented
Interpersonal communication skill
A good team player and good planner |
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