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Regulatory Medical Writer - work from home, Europe

Business Type: Contract Research Organisation
Job Type: Medical Writing and Editorial
Job Level: Experienced (non manager)
Position: Full Time
Location: Germany
Reference: KA286415_1
Closing Date: 23/04/21
Job Details:

I am helping one of my clients, one of the largest CRO''s, find new team members for their Medical Writing teams. Looking to speak both to Medical Writers and Senior Medical Writers.

The company is growing rapidly, yet offering very stable and secure job opportunities. The team is lovely and you will really feel like part of a family. They work a lot with Oncology, so if it is your area of interest - you will get an insanely good experience.

The Medical Writer will be working closely with the Senior Medical Writer and under the supervision of the Head of
Medical Affairs Unit, will be responsible for drafting, editing, and reviewing preclinical/clinical documents such as
preclinical and clinical study reports, study protocols, patient information, and informed consent forms, and
other medical and regulatory documents (including Investigators'' Brochure, IMPD, Briefing Document for
Scientific Advice and follow-up scientific advice, CTD).

This role can be fully remote (Europe)

To find out more, please send your resume to and I will get in touch.

Posted: 16/04/2021 | NPJ Ref: 269234 | NPJ Original URL
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