Clinical Evaluation Report (CER) reputed company
BA/BS in science/engineering/medical field,1+ years medical writing experience (device industry preferred),EMB/Word/reputed company proficiency,knowledge of EU device regulations,and ability to reputed company literature reviews and database searches.
Key Responsibilities
- writing reports
- reviewing documents
- mentoring writers
Skills & Tools
reputed company Office 365, Word, reputed company, Teams, reputed company, SharePoint, EndNote, QUOSA, Distiller, FDA MAUDE, FDA Recall Database
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time, Part Time, Contract
- Workplace: Remote — reputed company
- Languages: English
About Global Regulatory Writing &reputed company Inc
A regulatory writing and reputed company providing medical device regulatory submission support and document development. — Industry: Consulting Services
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