Medical Writer jobs in California
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SR. MEDICAL WRITER - 19909
BS degree required with 6+ years of recent experience specializing in quality systems and risk management. 10+ years of industry experience with quality systems management within biotech, pharma experience preferred,. Must be a S...
| Company | Simply Biotech |
|---|---|
| Address | San Francisco, CA |
| Category | Media & Communications |
| Job type | Full-Time |
| Date Posted | 3 weeks ago See detail |
Sr. Medical Writer - 19909
Simply Biotech
San Francisco, CA
BS degree required with 6+ years of recent experience specializing in quality systems and risk management. 10+ years of industry experience with quality systems management within biotech, pharma experience preferred,. Must be a S...
3 weeks ago seen See more...
- View all Simply Biotech jobs - jobs in San Francisco, CA
Medical Writer/ Sr. Medical Writer
Therapeutics Inc.
San Diego, CA
You will participate and supervise the development of clinical, regulatory, and scientific documents for publication and submission to regulatory agencies as well as be responsible for coordinating the contributions of the differe...
a month ago seen See more...
- View all Therapeutics Inc. jobs - jobs in San Diego, CA
Senior Medical Writer - 19863
Simply Biotech
San Francisco, CA
BS degree required, MS degree preferred, 4+ years of industry experience with medical writing internally at a biotech company. Must have experience with drafting SOP's regarding medical writing. Must have experience with drafting...
a month ago seen See more...
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Sr. Medical Writer
Microvention
Tustin, CA
Collaborating with the clinical & regulatory teams to write clinical documents for regulatory submissions, including but not limited to:Clinical evaluation reports.Interim and final clinical study reports.Briefing documents.Previo...
a month ago seen See more...
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Sr. Technical Writer - Medical Device Labeling
Boston Scientific
Valencia, CA
Author Medical Device Labeling deliverables. Manage, organize, and communicate project information and project activities. Apply corporate and regulatory Medical Device documentation requirements. Participate within, and possibly...
a month ago seen See more...
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